ClinVar Miner

Variants in gene combination LOC114827851, MYH6 with conflicting interpretations reported as "benign and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 13
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.166G>A (p.Gly56Arg) rs28711516 0.06950
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.622G>A (p.Asp208Asn) rs142027794 0.00415
NM_002471.4(MYH6):c.531-19T>A rs374174532 0.00045
NM_002471.4(MYH6):c.210T>C (p.Thr70=) rs147397431 0.00041
NM_002471.4(MYH6):c.420C>T (p.Ala140=) rs145023897 0.00010
NM_002471.4(MYH6):c.-8G>A rs28730779 0.00009
NM_002471.4(MYH6):c.252C>T (p.Phe84=) rs397516757 0.00001
NM_002471.4(MYH6):c.427C>A (p.Arg143=) rs2277473
NM_002471.4(MYH6):c.70C>A (p.Leu24Ile) rs573489857

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