rs730880947

Orientation

minus

Stabilized

minus

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

Make rs730880947(A;G)

Make rs730880947(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

110915771

Gene

MYL2

is a	snp
is	mentioned by
dbSNP	rs730880947
dbSNP (classic)	rs730880947
ClinGen	rs730880947
ebi	rs730880947
HLI	rs730880947
Exac	rs730880947
Gnomad	rs730880947
Varsome	rs730880947
LitVar	rs730880947
Map	rs730880947
PheGenI	rs730880947
Biobank	rs730880947
1000 genomes	rs730880947
hgdp	rs730880947
ensembl	rs730880947
geneview	rs730880947
scholar	rs730880947
google	rs730880947
pharmgkb	rs730880947
gwascentral	rs730880947
openSNP	rs730880947
23andMe	rs730880947
SNPshot	rs730880947
SNPdbe	rs730880947
MSV3d	rs730880947
GWAS Ctlg	rs730880947

Max Magnitude

0

ClinVar
Risk	rs730880947(G;G)
Alt	rs730880947(G;G)
Reference	Rs730880947(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYL2
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.111353575T>C
CLNSRC
CLNACC	RCV000158918.2,