rs375667565

Orientation

plus

Stabilized

plus

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

Make rs375667565(A;A)

Make rs375667565(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

110913124

Gene

MYL2

is a	snp
is	mentioned by
dbSNP	rs375667565
dbSNP (classic)	rs375667565
ClinGen	rs375667565
ebi	rs375667565
HLI	rs375667565
Exac	rs375667565
Gnomad	rs375667565
Varsome	rs375667565
LitVar	rs375667565
Map	rs375667565
PheGenI	rs375667565
Biobank	rs375667565
1000 genomes	rs375667565
hgdp	rs375667565
ensembl	rs375667565
geneview	rs375667565
scholar	rs375667565
google	rs375667565
pharmgkb	rs375667565
gwascentral	rs375667565
openSNP	rs375667565
23andMe	rs375667565
SNPshot	rs375667565
SNPdbe	rs375667565
MSV3d	rs375667565
GWAS Ctlg	rs375667565

Max Magnitude

0

ClinVar
Risk	rs375667565(A;A)
Alt	rs375667565(A;A)
Reference	Rs375667565(G;G)
Significance	Probable-Pathogenic
Disease	not specified Cardiomyopathy
Variation	info
Gene	MYL2
CLNDBN	not specified Cardiomyopathy
Reversed	0
HGVS	NC_000012.11:g.111350928G>A
CLNSRC
CLNACC	RCV000036400.3, RCV000157370.2,