rs121434593

Orientation

minus

Stabilized

minus

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

Make rs121434593(A;A)

Make rs121434593(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

40237979

Gene

AKT2

is a	snp
is	mentioned by
dbSNP	rs121434593
dbSNP (classic)	rs121434593
ClinGen	rs121434593
ebi	rs121434593
HLI	rs121434593
Exac	rs121434593
Gnomad	rs121434593
Varsome	rs121434593
LitVar	rs121434593
Map	rs121434593
PheGenI	rs121434593
Biobank	rs121434593
1000 genomes	rs121434593
hgdp	rs121434593
ensembl	rs121434593
geneview	rs121434593
scholar	rs121434593
google	rs121434593
pharmgkb	rs121434593
gwascentral	rs121434593
openSNP	rs121434593
23andMe	rs121434593
SNPshot	rs121434593
SNPdbe	rs121434593
MSV3d	rs121434593
GWAS Ctlg	rs121434593

Max Magnitude

0

OMIM	164731
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121434593(A;A)
Alt	rs121434593(A;A)
Reference	Rs121434593(G;G)
Significance	Pathogenic
Disease	Diabetes mellitus type 2
Variation	info
Gene	AKT2
CLNDBN	Diabetes mellitus type 2
Reversed	1
HGVS	NC_000019.9:g.40743886C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015016.25,