rs587782965

Orientation

minus

Stabilized

minus

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

Make rs587782965(A;A)

Make rs587782965(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

110914221

Gene

MYL2

is a	snp
is	mentioned by
dbSNP	rs587782965
dbSNP (classic)	rs587782965
ClinGen	rs587782965
ebi	rs587782965
HLI	rs587782965
Exac	rs587782965
Gnomad	rs587782965
Varsome	rs587782965
LitVar	rs587782965
Map	rs587782965
PheGenI	rs587782965
Biobank	rs587782965
1000 genomes	rs587782965
hgdp	rs587782965
ensembl	rs587782965
geneview	rs587782965
scholar	rs587782965
google	rs587782965
pharmgkb	rs587782965
gwascentral	rs587782965
openSNP	rs587782965
23andMe	rs587782965
SNPshot	rs587782965
SNPdbe	rs587782965
MSV3d	rs587782965
GWAS Ctlg	rs587782965

Max Magnitude

0

ClinVar
Risk	rs587782965(A;A)
Alt	rs587782965(A;A)
Reference	Rs587782965(C;C)
Significance	Probable-Pathogenic
Disease	Primary familial hypertrophic cardiomyopathy
Variation	info
Gene	MYL2
CLNDBN	Primary familial hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000012.11:g.111352025G>T
CLNSRC
CLNACC	RCV000143928.2,