rs150634297

Orientation

plus

Stabilized

plus

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

Make rs150634297(C;T)

Make rs150634297(T;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

46860748

Gene

MYL3

is a	snp
is	mentioned by
dbSNP	rs150634297
dbSNP (classic)	rs150634297
ClinGen	rs150634297
ebi	rs150634297
HLI	rs150634297
Exac	rs150634297
Gnomad	rs150634297
Varsome	rs150634297
LitVar	rs150634297
Map	rs150634297
PheGenI	rs150634297
Biobank	rs150634297
1000 genomes	rs150634297
hgdp	rs150634297
ensembl	rs150634297
geneview	rs150634297
scholar	rs150634297
google	rs150634297
pharmgkb	rs150634297
gwascentral	rs150634297
openSNP	rs150634297
23andMe	rs150634297
SNPshot	rs150634297
SNPdbe	rs150634297
MSV3d	rs150634297
GWAS Ctlg	rs150634297

Max Magnitude

0

ClinVar
Risk	rs150634297(T;T)
Alt	rs150634297(T;T)
Reference	Rs150634297(C;C)
Significance	Probable-Pathogenic
Disease	Primary familial hypertrophic cardiomyopathy
Variation	info
Gene	MYL3
CLNDBN	Primary familial hypertrophic cardiomyopathy
Reversed	0
HGVS	NC_000003.11:g.46902238C>T
CLNSRC	ClinVar University of Washington
CLNACC	RCV000148716.1,