RS11666328 MYH14

Health Risk Chr 19:50232082 snv intron variant
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Associated Conditions
Autosomal dominant nonsyndromic hearing loss 4A
Autosomal dominant nonsyndromic hearing loss 4A
Population Frequencies
gnomAD ALL
63.4%
1kG AFR
78.1%
1kG ALL
32.1%
1kG AMR
67.7%
1kG EAS
65.4%
1kG EUR
36%
1kG SAS
60.6%
Other Variants in MYH14
rs119103279 rs28940307 rs119103280 rs119103281 rs113993956 rs142696359 rs397516628 rs397516629 rs200272339 rs200878464
Ask Dr. Hemsworth about this variant