RS1137617 KCNH2

Health Risk Chr 7:150951109 snv stop gained
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What This Variant Does
"rs1137617 represents a variant in the KCNH2 gene on chromosome 7. There are several reported alleles...
Associated Conditions
Long QT syndrome
Ovarian serous cystadenocarcinoma
Long QT syndrome
Ovarian serous cystadenocarcinoma
Population Frequencies
gnomAD ALL
37%
1kG AFR
94.5%
1kG ALL
77.2%
1kG AMR
63.8%
1kG EAS
11.8%
1kG EUR
60.4%
1kG SAS
69.3%
Other Variants in KCNH2
rs121912504 rs121912505 rs28928904 rs121912506 rs1554426258 rs121912507 rs121912508 rs9333649 rs28928905 rs121912509
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