rs397516186

Orientation

minus

Stabilized

minus

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

Make rs397516186(A;A)

Make rs397516186(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23420107

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs397516186
dbSNP (classic)	rs397516186
ClinGen	rs397516186
ebi	rs397516186
HLI	rs397516186
Exac	rs397516186
Gnomad	rs397516186
Varsome	rs397516186
LitVar	rs397516186
Map	rs397516186
PheGenI	rs397516186
Biobank	rs397516186
1000 genomes	rs397516186
hgdp	rs397516186
ensembl	rs397516186
geneview	rs397516186
scholar	rs397516186
google	rs397516186
pharmgkb	rs397516186
gwascentral	rs397516186
openSNP	rs397516186
23andMe	rs397516186
SNPshot	rs397516186
SNPdbe	rs397516186
MSV3d	rs397516186
GWAS Ctlg	rs397516186

Max Magnitude

0

ClinVar
Risk	rs397516186(A;A)
Alt	rs397516186(A;A)
Reference	Rs397516186(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23889316C>T
CLNSRC	ClinVar
CLNACC	RCV000035857.4,