ClinVar Miner

List of variants reported as benign for autosomal dominant nonsyndromic hearing loss 17 by Illumina Laboratory Services, Illumina

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_002473.6(MYH9):c.3429T>G (p.Ala1143=) rs710181 0.97278
NM_002473.6(MYH9):c.1728+10G>A rs2413396 0.77118
NM_002473.6(MYH9):c.1554+7A>G rs3752462 0.53193
NM_002473.6(MYH9):c.*596G>A rs136200 0.32779
NM_002473.6(MYH9):c.*261G>C rs11089787 0.25506
NM_002473.6(MYH9):c.*800T>C rs7078 0.23633
NM_002473.6(MYH9):c.*238G>T rs11703176 0.22062
NM_002473.6(MYH9):c.4876A>G (p.Ile1626Val) rs2269529 0.17342
NM_002473.6(MYH9):c.4872G>T (p.Ala1624=) rs2269530 0.17309
NM_002473.6(MYH9):c.*732C>T rs12107 0.16843
NM_002473.6(MYH9):c.*1314C>T rs2481 0.15103
NM_002473.6(MYH9):c.4899G>A (p.Arg1633=) rs5756130 0.07263
NM_002473.6(MYH9):c.2256T>C (p.Asn752=) rs9619601 0.04672
NM_002473.6(MYH9):c.3345A>G (p.Glu1115=) rs875725 0.03292
NM_002473.6(MYH9):c.4563C>T (p.His1521=) rs11549907 0.02903
NM_002473.6(MYH9):c.3100+11G>C rs41279999 0.02869
NM_002473.6(MYH9):c.*312C>T rs16996639 0.02830
NM_002473.6(MYH9):c.*137C>A rs114268057 0.02699
NM_002473.6(MYH9):c.*136C>A rs115869378 0.02697
NM_002473.6(MYH9):c.3838-8C>T rs145429636 0.02315
NM_002473.6(MYH9):c.3838-12C>T rs113698937 0.01529
NM_002473.6(MYH9):c.1626C>T (p.Phe542=) rs7285745 0.01011
NM_002473.6(MYH9):c.*243C>T rs136201 0.00965
NM_002473.6(MYH9):c.1108+9C>T rs145751072 0.00959
NM_002473.6(MYH9):c.2038-5T>C rs8137674 0.00874
NM_002473.6(MYH9):c.1729-6C>T rs9622375 0.00736
NM_002473.6(MYH9):c.5815G>A (p.Ala1939Thr) rs115031369 0.00508
NM_002473.6(MYH9):c.1083C>T (p.Asp361=) rs56001030 0.00436
NM_002473.6(MYH9):c.2721C>T (p.Thr907=) rs148112044 0.00435
NM_002473.6(MYH9):c.3485+8C>T rs149559551 0.00193
NM_002473.6(MYH9):c.2517G>A (p.Gln839=) rs34498733 0.00038
NM_002473.6(MYH9):c.*906G>T rs192511111 0.00030
NM_002473.6(MYH9):c.18C>T (p.Ala6=) rs141055332 0.00021
NM_002473.6(MYH9):c.5483+4C>G rs56327920
NM_002473.6(MYH9):c.5781G>T (p.Pro1927=) rs80050551

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