rs397516372

Orientation

plus

Stabilized

plus

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

Make rs397516372(C;G)

Make rs397516372(G;G)

Reference

GRCh38 38.1/141

Chromosome

15

Position

63059645

Gene

TPM1

is a	snp
is	mentioned by
dbSNP	rs397516372
dbSNP (classic)	rs397516372
ClinGen	rs397516372
ebi	rs397516372
HLI	rs397516372
Exac	rs397516372
Gnomad	rs397516372
Varsome	rs397516372
LitVar	rs397516372
Map	rs397516372
PheGenI	rs397516372
Biobank	rs397516372
1000 genomes	rs397516372
hgdp	rs397516372
ensembl	rs397516372
geneview	rs397516372
scholar	rs397516372
google	rs397516372
pharmgkb	rs397516372
gwascentral	rs397516372
openSNP	rs397516372
23andMe	rs397516372
SNPshot	rs397516372
SNPdbe	rs397516372
MSV3d	rs397516372
GWAS Ctlg	rs397516372

Max Magnitude

0

ClinVar
Risk	rs397516372(G;G)
Alt	rs397516372(G;G)
Reference	Rs397516372(C;C)
Significance	Probable-Pathogenic
Disease	Primary familial hypertrophic cardiomyopathy
Variation	info
Gene	TPM1
CLNDBN	Primary familial hypertrophic cardiomyopathy
Reversed	0
HGVS	NC_000015.9:g.63351844C>G
CLNSRC	ClinVar
CLNACC	RCV000036333.2,