| Phenotype Name |
Clinical Significance |
dbSNP ID |
RCV Accession |
| Clear cell carcinoma of kidney |
Benign; Likely benign |
rs144426436 |
RCV005892276 |
| Complex neurodevelopmental disorder |
Conflicting classifications of pathogenicity |
rs778642222 |
RCV005361108 |
| EPB41L1-related disorder |
Benign; Likely benign; Uncertain significance |
rs2295568, rs147654123, rs144426436, rs145893462, rs1600984787, rs2063036322, rs150389879, rs756577865, rs766993119, rs201212477, rs574706898, rs78442416 |
RCV003975020 RCV003907683 RCV003977512 RCV003919002 RCV003894535 RCV003896361 RCV003933924 RCV003944065 RCV003934748 RCV003957253 RCV003969186 RCV003960162 |
| Gastric cancer |
Benign; Likely benign |
rs144426436 |
RCV005892277 |
| Intellectual disability |
Likely benign |
rs1242238241, rs375772370, rs2063600623 |
RCV001252245 RCV001252244 RCV001252480 |
| Intellectual disability, autosomal dominant 11 |
Uncertain significance; Conflicting classifications of pathogenicity; no classifications from unflagged records |
rs2063022720, rs2147709505, rs2145899366, rs2063017244, rs2516820666, rs778642222, rs2516006807, rs1569376434, rs1569330133, rs766068292 |
RCV001328644 RCV001733557 RCV001837353 RCV002467415 RCV002472171 RCV004783760 RCV004566624 RCV000023216 RCV000679982 RCV001198025 |
| Lung cancer |
Benign; Likely benign |
rs144426436 |
RCV005892279 |
| Malignant tumor of esophagus |
Benign; Likely benign |
rs144426436 |
RCV005892274 |
| Malignant tumor of urinary bladder |
Benign; Likely benign |
rs144426436, rs146637110 |
RCV005892273 RCV005902919 |
| Nonpapillary renal cell carcinoma |
Benign; Likely benign |
rs144426436 |
RCV005892275 |
| Ovarian serous cystadenocarcinoma |
Benign; Likely benign |
rs144426436, rs146637110 |
RCV005892278 RCV005902920 |