rs397516165

Orientation

minus

Stabilized

minus

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

Make rs397516165(A;A)

Make rs397516165(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23424118

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs397516165
dbSNP (classic)	rs397516165
ClinGen	rs397516165
ebi	rs397516165
HLI	rs397516165
Exac	rs397516165
Gnomad	rs397516165
Varsome	rs397516165
LitVar	rs397516165
Map	rs397516165
PheGenI	rs397516165
Biobank	rs397516165
1000 genomes	rs397516165
hgdp	rs397516165
ensembl	rs397516165
geneview	rs397516165
scholar	rs397516165
google	rs397516165
pharmgkb	rs397516165
gwascentral	rs397516165
openSNP	rs397516165
23andMe	rs397516165
SNPshot	rs397516165
SNPdbe	rs397516165
MSV3d	rs397516165
GWAS Ctlg	rs397516165

Max Magnitude

0

ClinVar
Risk	rs397516165(A;A) rs397516165(C;C)
Alt	rs397516165(A;A) rs397516165(C;C)
Reference	Rs397516165(G;G)
Significance	Probable-Pathogenic
Disease	not specified Primary dilated cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	not specified Primary dilated cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23893327C>T
CLNSRC	ClinVar
CLNACC	RCV000035816.2, RCV000208309.1,