rs397516103

Orientation

minus

Stabilized

minus

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

Make rs397516103(C;C)

Make rs397516103(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23428992

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs397516103
dbSNP (classic)	rs397516103
ClinGen	rs397516103
ebi	rs397516103
HLI	rs397516103
Exac	rs397516103
Gnomad	rs397516103
Varsome	rs397516103
LitVar	rs397516103
Map	rs397516103
PheGenI	rs397516103
Biobank	rs397516103
1000 genomes	rs397516103
hgdp	rs397516103
ensembl	rs397516103
geneview	rs397516103
scholar	rs397516103
google	rs397516103
pharmgkb	rs397516103
gwascentral	rs397516103
openSNP	rs397516103
23andMe	rs397516103
SNPshot	rs397516103
SNPdbe	rs397516103
MSV3d	rs397516103
GWAS Ctlg	rs397516103

Max Magnitude

0

ClinVar
Risk	rs397516103(C;C)
Alt	rs397516103(C;C)
Reference	Rs397516103(T;T)
Significance	Pathogenic
Disease	not specified Hypertrophic cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	not specified Hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23898201A>G
CLNSRC	ClinVar
CLNACC	RCV000035720.3, RCV000477379.1,