ClinVar Miner

List of variants in gene LOC114827851, MYH6 studied for Cardiomyopathy

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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.399G>A (p.Val133=) rs78891557 0.01343
NM_002471.4(MYH6):c.330G>A (p.Ala110=) rs77679218 0.00490
NM_002471.4(MYH6):c.36G>A (p.Ala12=) rs141014719 0.00487
NM_002471.4(MYH6):c.86G>A (p.Arg29Gln) rs150574114 0.00455
NM_002471.4(MYH6):c.-5C>A rs183611755 0.00438
NM_002471.4(MYH6):c.622G>A (p.Asp208Asn) rs142027794 0.00417
NM_002471.4(MYH6):c.292G>A (p.Glu98Lys) rs140596256 0.00030
NM_002471.4(MYH6):c.408C>T (p.Ala136=) rs140732380 0.00025
NM_002471.4(MYH6):c.70C>A (p.Leu24Ile) rs573489857 0.00015
NM_002471.4(MYH6):c.420C>T (p.Ala140=) rs145023897 0.00010
NM_002471.4(MYH6):c.636G>A (p.Ala212=) rs111265123 0.00003
NM_002471.4(MYH6):c.354G>A (p.Ser118=) rs373427673 0.00002
NM_002471.4(MYH6):c.642+1G>C rs199989693 0.00001
NM_002471.4(MYH6):c.68G>A (p.Arg23His) rs771786844 0.00001
NM_002471.4(MYH6):c.105T>C (p.Thr35=) rs1345462210
NM_002471.4(MYH6):c.503-8T>C rs1566516373
NM_002471.4(MYH6):c.601A>G (p.Ile201Val) rs1891728161
NM_002471.4(MYH6):c.642+3G>A rs374013248

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