rs730880950

Orientation

minus

Stabilized

minus

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

Make rs730880950(C;C)

Make rs730880950(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

110914203

Gene

MYL2

is a	snp
is	mentioned by
dbSNP	rs730880950
dbSNP (classic)	rs730880950
ClinGen	rs730880950
ebi	rs730880950
HLI	rs730880950
Exac	rs730880950
Gnomad	rs730880950
Varsome	rs730880950
LitVar	rs730880950
Map	rs730880950
PheGenI	rs730880950
Biobank	rs730880950
1000 genomes	rs730880950
hgdp	rs730880950
ensembl	rs730880950
geneview	rs730880950
scholar	rs730880950
google	rs730880950
pharmgkb	rs730880950
gwascentral	rs730880950
openSNP	rs730880950
23andMe	rs730880950
SNPshot	rs730880950
SNPdbe	rs730880950
MSV3d	rs730880950
GWAS Ctlg	rs730880950

Max Magnitude

0

ClinVar
Risk	rs730880950(C;C)
Alt	rs730880950(C;C)
Reference	Rs730880950(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYL2
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.111352007A>G
CLNSRC
CLNACC	RCV000158925.1,