rs1057517773

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1057517773(A;A)

Make rs1057517773(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

23431641

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs1057517773
dbSNP (classic)	rs1057517773
ClinGen	rs1057517773
ebi	rs1057517773
HLI	rs1057517773
Exac	rs1057517773
Gnomad	rs1057517773
Varsome	rs1057517773
LitVar	rs1057517773
Map	rs1057517773
PheGenI	rs1057517773
Biobank	rs1057517773
1000 genomes	rs1057517773
hgdp	rs1057517773
ensembl	rs1057517773
geneview	rs1057517773
scholar	rs1057517773
google	rs1057517773
pharmgkb	rs1057517773
gwascentral	rs1057517773
openSNP	rs1057517773
23andMe	rs1057517773
SNPshot	rs1057517773
SNPdbe	rs1057517773
MSV3d	rs1057517773
GWAS Ctlg	rs1057517773

Max Magnitude

0

ClinVar
Risk	rs1057517773(A;A)
Alt	rs1057517773(A;A)
Reference	Rs1057517773(G;G)
Significance	Probable-Pathogenic
Disease	not specified Hypertrophic cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	not specified Hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23900850C>T
CLNSRC
CLNACC	RCV000412779.1, RCV000457952.1,