rs869025485

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;G)	6.2	Familial Hypertrophic Cardiomyopathy
(G;G)	0	common in clinvar

Make rs869025485(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

46859573

Gene

MYL3

is a	snp
is	mentioned by
dbSNP	rs869025485
dbSNP (classic)	rs869025485
ClinGen	rs869025485
ebi	rs869025485
HLI	rs869025485
Exac	rs869025485
Gnomad	rs869025485
Varsome	rs869025485
LitVar	rs869025485
Map	rs869025485
PheGenI	rs869025485
Biobank	rs869025485
1000 genomes	rs869025485
hgdp	rs869025485
ensembl	rs869025485
geneview	rs869025485
scholar	rs869025485
google	rs869025485
pharmgkb	rs869025485
gwascentral	rs869025485
openSNP	rs869025485
23andMe	rs869025485
SNPshot	rs869025485
SNPdbe	rs869025485
MSV3d	rs869025485
GWAS Ctlg	rs869025485

Max Magnitude

6.2

ClinVar
Risk	rs869025485(A;A)
Alt	rs869025485(A;A)
Reference	Rs869025485(G;G)
Significance	Probable-Pathogenic
Disease	Primary familial hypertrophic cardiomyopathy
Variation	info
Gene	MYL3
CLNDBN	Primary familial hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000003.11:g.46901063C>T
CLNSRC
CLNACC	RCV000208278.1,