rs730880944

Orientation

minus

Stabilized

minus

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

Make rs730880944(C;C)

Make rs730880944(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

110919144

Gene

MYL2

is a	snp
is	mentioned by
dbSNP	rs730880944
dbSNP (classic)	rs730880944
ClinGen	rs730880944
ebi	rs730880944
HLI	rs730880944
Exac	rs730880944
Gnomad	rs730880944
Varsome	rs730880944
LitVar	rs730880944
Map	rs730880944
PheGenI	rs730880944
Biobank	rs730880944
1000 genomes	rs730880944
hgdp	rs730880944
ensembl	rs730880944
geneview	rs730880944
scholar	rs730880944
google	rs730880944
pharmgkb	rs730880944
gwascentral	rs730880944
openSNP	rs730880944
23andMe	rs730880944
SNPshot	rs730880944
SNPdbe	rs730880944
MSV3d	rs730880944
GWAS Ctlg	rs730880944

Max Magnitude

0

ClinVar
Risk	rs730880944(C;C)
Alt	rs730880944(C;C)
Reference	Rs730880944(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MYL2
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.111356948A>G
CLNSRC
CLNACC	RCV000158913.2,