| Phenotype Name |
Clinical Significance |
dbSNP ID |
RCV Accession |
| Acute myeloid leukemia |
Benign |
rs78364534 |
RCV005923501 |
| Cervical cancer |
Likely benign |
rs77841771 |
RCV005919251 |
| Cholangiocarcinoma |
Benign |
rs78364534 |
RCV005923506 |
| CIT-related disorder |
Uncertain significance; Likely benign; Benign; Conflicting classifications of pathogenicity |
rs548588963, rs776480559, rs139602765, rs190275140, rs138651199, rs201139538, rs200757503, rs146054076, rs199767013, rs959207549, rs754251381, rs766786434, rs377149379, rs367918257, rs143040240, rs946466934, rs755717565, rs2136979223, rs748717608, rs779034565, rs779412220, rs1301165297, rs755628356, rs765245518, rs1489315183, rs56006347, rs79892909, rs145731510, rs35431237, rs149158991, rs61735286, rs138430777, rs139308004, rs56193743, rs574844028, rs116251862, rs186505065, rs758358701, rs571765841, rs186244485, rs557478027, rs112550001, rs373076345, rs780981739, rs200613360 View all (30 more) |
RCV003931180 RCV003956243 RCV004757479 RCV003933693 RCV003953860 RCV003963622 RCV003946269 RCV003906522 RCV003936459 RCV003900991 RCV003900992 RCV003909002 RCV003946720 RCV003919362 RCV003939269 RCV003896656 RCV003896823 RCV003923906 RCV003977125 RCV003961735 RCV003914667 RCV003939535 RCV003934770 RCV003924456 RCV003959151 RCV003934607 RCV003902764 RCV003938159 RCV003970818 RCV003962916 RCV003975521 RCV003967962 RCV003975535 RCV003940588 RCV003968129 RCV003923063 RCV003950703 RCV003960398 RCV003903009 RCV003978009 RCV003970377 RCV003960451 RCV003903027 RCV003913159 RCV003928604 |
| Clear cell carcinoma of kidney |
Conflicting classifications of pathogenicity; Uncertain significance |
rs142607751, rs144005700 |
RCV005911433 RCV005931044 |
| Colon adenocarcinoma |
Conflicting classifications of pathogenicity |
rs142607751 |
RCV005911432 |
| Familial cancer of breast |
Conflicting classifications of pathogenicity |
rs142607751 |
RCV005911431 |
| Gastric cancer |
Conflicting classifications of pathogenicity; Likely benign |
rs142607751, rs77841771, rs146054076 |
RCV005911434 RCV005919253 RCV005930541 |
| Intellectual disability |
Conflicting classifications of pathogenicity |
rs771292782, rs145731510 |
RCV005625693 RCV005626210 |
| Long QT syndrome |
Uncertain significance |
rs796052161, rs776383369 |
RCV000190154 RCV000190241 |
| Lung cancer |
Likely benign |
rs77841771 |
RCV005919255 |
| Malignant tumor of esophagus |
Benign |
rs78364534 |
RCV005923502 |
| Marfanoid habitus and intellectual disability |
Uncertain significance |
rs1593428225 |
RCV000850446 |
| Melanoma |
Conflicting classifications of pathogenicity |
rs142607751 |
RCV005911435 |
| Ovarian serous cystadenocarcinoma |
Likely benign; Benign |
rs77841771, rs9738242 |
RCV005919254 RCV005917189 |
| Sarcoma |
Likely benign; Benign; Uncertain significance |
rs138689173, rs73215386, rs77841771, rs78364534, rs116965587 |
RCV005915970 RCV005916095 RCV005919252 RCV005923503 RCV005939142 |
| See cases |
Uncertain significance |
rs2500851231 |
RCV003128534 |
| Thymoma |
Benign |
rs78364534 |
RCV005923505 |
| Uterine carcinosarcoma |
Likely benign; Benign |
rs73215386, rs78364534 |
RCV005916096 RCV005923504 |
| Uterine corpus endometrial carcinoma |
Likely benign; Benign |
rs77841771, rs9738242 |
RCV005919256 RCV005917190 |
|