rs397516341

Orientation

minus

Stabilized

minus

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

Make rs397516341(A;G)

Make rs397516341(G;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

55157589

Gene	LOC101930593, TNNI3

is a	snp
is	mentioned by
dbSNP	rs397516341
dbSNP (classic)	rs397516341
ClinGen	rs397516341
ebi	rs397516341
HLI	rs397516341
Exac	rs397516341
Gnomad	rs397516341
Varsome	rs397516341
LitVar	rs397516341
Map	rs397516341
PheGenI	rs397516341
Biobank	rs397516341
1000 genomes	rs397516341
hgdp	rs397516341
ensembl	rs397516341
geneview	rs397516341
scholar	rs397516341
google	rs397516341
pharmgkb	rs397516341
gwascentral	rs397516341
openSNP	rs397516341
23andMe	rs397516341
SNPshot	rs397516341
SNPdbe	rs397516341
MSV3d	rs397516341
GWAS Ctlg	rs397516341

Max Magnitude

0

ClinVar
Risk	rs397516341(G;G)
Alt	rs397516341(G;G)
Reference	Rs397516341(A;A)
Significance	Probable-Pathogenic
Disease	Primary familial hypertrophic cardiomyopathy
Variation	info
Gene	TNNI3
CLNDBN	Primary familial hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000019.9:g.55668957T>C
CLNSRC	ClinVar
CLNACC	RCV000036273.2,