rs397516249

Orientation

minus

Stabilized

minus

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

Make rs397516249(A;G)

Make rs397516249(G;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23431840

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs397516249
dbSNP (classic)	rs397516249
ClinGen	rs397516249
ebi	rs397516249
HLI	rs397516249
Exac	rs397516249
Gnomad	rs397516249
Varsome	rs397516249
LitVar	rs397516249
Map	rs397516249
PheGenI	rs397516249
Biobank	rs397516249
1000 genomes	rs397516249
hgdp	rs397516249
ensembl	rs397516249
geneview	rs397516249
scholar	rs397516249
google	rs397516249
pharmgkb	rs397516249
gwascentral	rs397516249
openSNP	rs397516249
23andMe	rs397516249
SNPshot	rs397516249
SNPdbe	rs397516249
MSV3d	rs397516249
GWAS Ctlg	rs397516249

Max Magnitude

0

ClinVar
Risk	rs397516249(G;G)
Alt	rs397516249(G;G)
Reference	Rs397516249(A;A)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23901049T>C
CLNSRC	ClinVar
CLNACC	RCV000035972.3,