rs730880948

Orientation

minus

Stabilized

minus

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

Make rs730880948(G;T)

Make rs730880948(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

110920526

Gene

MYL2

is a	snp
is	mentioned by
dbSNP	rs730880948
dbSNP (classic)	rs730880948
ClinGen	rs730880948
ebi	rs730880948
HLI	rs730880948
Exac	rs730880948
Gnomad	rs730880948
Varsome	rs730880948
LitVar	rs730880948
Map	rs730880948
PheGenI	rs730880948
Biobank	rs730880948
1000 genomes	rs730880948
hgdp	rs730880948
ensembl	rs730880948
geneview	rs730880948
scholar	rs730880948
google	rs730880948
pharmgkb	rs730880948
gwascentral	rs730880948
openSNP	rs730880948
23andMe	rs730880948
SNPshot	rs730880948
SNPdbe	rs730880948
MSV3d	rs730880948
GWAS Ctlg	rs730880948

Max Magnitude

0

ClinVar
Risk	rs730880948(T;T)
Alt	rs730880948(T;T)
Reference	Rs730880948(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MYL2
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.111358330C>A
CLNSRC
CLNACC	RCV000158921.2,