rs1057517771

Orientation

minus

Stabilized

minus

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

Make rs1057517771(A;G)

Make rs1057517771(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

23432656

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs1057517771
dbSNP (classic)	rs1057517771
ClinGen	rs1057517771
ebi	rs1057517771
HLI	rs1057517771
Exac	rs1057517771
Gnomad	rs1057517771
Varsome	rs1057517771
LitVar	rs1057517771
Map	rs1057517771
PheGenI	rs1057517771
Biobank	rs1057517771
1000 genomes	rs1057517771
hgdp	rs1057517771
ensembl	rs1057517771
geneview	rs1057517771
scholar	rs1057517771
google	rs1057517771
pharmgkb	rs1057517771
gwascentral	rs1057517771
openSNP	rs1057517771
23andMe	rs1057517771
SNPshot	rs1057517771
SNPdbe	rs1057517771
MSV3d	rs1057517771
GWAS Ctlg	rs1057517771

Max Magnitude

0

ClinVar
Risk	rs1057517771(G;G)
Alt	rs1057517771(G;G)
Reference	Rs1057517771(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23901865T>C
CLNSRC
CLNACC	RCV000413559.1,