rs121913150

Orientation

minus

Stabilized

minus

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

Make rs121913150(A;A)

Make rs121913150(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

7120707

Gene

INSR

is a	snp
is	mentioned by
dbSNP	rs121913150
dbSNP (classic)	rs121913150
ClinGen	rs121913150
ebi	rs121913150
HLI	rs121913150
Exac	rs121913150
Gnomad	rs121913150
Varsome	rs121913150
LitVar	rs121913150
Map	rs121913150
PheGenI	rs121913150
Biobank	rs121913150
1000 genomes	rs121913150
hgdp	rs121913150
ensembl	rs121913150
geneview	rs121913150
scholar	rs121913150
google	rs121913150
pharmgkb	rs121913150
gwascentral	rs121913150
openSNP	rs121913150
23andMe	rs121913150
SNPshot	rs121913150
SNPdbe	rs121913150
MSV3d	rs121913150
GWAS Ctlg	rs121913150

Max Magnitude

0

OMIM	147670
Desc
Variant	0021
Related	also

ClinVar
Risk	rs121913150(A;A)
Alt	rs121913150(A;A)
Reference	Rs121913150(G;G)
Significance	Pathogenic
Disease	Diabetes mellitus type 2
Variation	info
Gene	INSR
CLNDBN	Diabetes mellitus type 2
Reversed	1
HGVS	NC_000019.9:g.7120718C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015815.30,