rs730880952

Orientation

minus

Stabilized

minus

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

Make rs730880952(G;T)

Make rs730880952(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

110911082

Gene

MYL2

is a	snp
is	mentioned by
dbSNP	rs730880952
dbSNP (classic)	rs730880952
ClinGen	rs730880952
ebi	rs730880952
HLI	rs730880952
Exac	rs730880952
Gnomad	rs730880952
Varsome	rs730880952
LitVar	rs730880952
Map	rs730880952
PheGenI	rs730880952
Biobank	rs730880952
1000 genomes	rs730880952
hgdp	rs730880952
ensembl	rs730880952
geneview	rs730880952
scholar	rs730880952
google	rs730880952
pharmgkb	rs730880952
gwascentral	rs730880952
openSNP	rs730880952
23andMe	rs730880952
SNPshot	rs730880952
SNPdbe	rs730880952
MSV3d	rs730880952
GWAS Ctlg	rs730880952

Max Magnitude

0

ClinVar
Risk	rs730880952(T;T)
Alt	rs730880952(T;T)
Reference	Rs730880952(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYL2
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.111348886C>A
CLNSRC
CLNACC	RCV000158935.2,