rs397516390

Orientation

plus

Stabilized

plus

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

Make rs397516390(A;G)

Make rs397516390(G;G)

Reference

GRCh38 38.1/141

Chromosome

15

Position

63064081

Gene

TPM1

is a	snp
is	mentioned by
dbSNP	rs397516390
dbSNP (classic)	rs397516390
ClinGen	rs397516390
ebi	rs397516390
HLI	rs397516390
Exac	rs397516390
Gnomad	rs397516390
Varsome	rs397516390
LitVar	rs397516390
Map	rs397516390
PheGenI	rs397516390
Biobank	rs397516390
1000 genomes	rs397516390
hgdp	rs397516390
ensembl	rs397516390
geneview	rs397516390
scholar	rs397516390
google	rs397516390
pharmgkb	rs397516390
gwascentral	rs397516390
openSNP	rs397516390
23andMe	rs397516390
SNPshot	rs397516390
SNPdbe	rs397516390
MSV3d	rs397516390
GWAS Ctlg	rs397516390

Max Magnitude

0

ClinVar
Risk	rs397516390(G;G)
Alt	rs397516390(G;G)
Reference	Rs397516390(A;A)
Significance	Probable-Pathogenic
Disease	Primary familial hypertrophic cardiomyopathy
Variation	info
Gene	TPM1
CLNDBN	Primary familial hypertrophic cardiomyopathy
Reversed	0
HGVS	NC_000015.9:g.63356280A>G
CLNSRC	ClinVar
CLNACC	RCV000036361.2,