rs397516097

Orientation

minus

Stabilized

minus

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

Make rs397516097(A;A)

Make rs397516097(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23429089

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs397516097
dbSNP (classic)	rs397516097
ClinGen	rs397516097
ebi	rs397516097
HLI	rs397516097
Exac	rs397516097
Gnomad	rs397516097
Varsome	rs397516097
LitVar	rs397516097
Map	rs397516097
PheGenI	rs397516097
Biobank	rs397516097
1000 genomes	rs397516097
hgdp	rs397516097
ensembl	rs397516097
geneview	rs397516097
scholar	rs397516097
google	rs397516097
pharmgkb	rs397516097
gwascentral	rs397516097
openSNP	rs397516097
23andMe	rs397516097
SNPshot	rs397516097
SNPdbe	rs397516097
MSV3d	rs397516097
GWAS Ctlg	rs397516097

Max Magnitude

0

ClinVar
Risk	rs397516097(A;A)
Alt	rs397516097(A;A)
Reference	Rs397516097(G;G)
Significance	Probable-Pathogenic
Disease	Primary familial hypertrophic cardiomyopathy not specified
Variation	info
Gene	MYH7
CLNDBN	Primary familial hypertrophic cardiomyopathy not specified
Reversed	1
HGVS	NC_000014.8:g.23898298C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000035712.2, RCV000158792.2,