rs121913157

Orientation

minus

Stabilized

minus

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

Make rs121913157(A;A)

Make rs121913157(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

7120739

Gene

INSR

is a	snp
is	mentioned by
dbSNP	rs121913157
dbSNP (classic)	rs121913157
ClinGen	rs121913157
ebi	rs121913157
HLI	rs121913157
Exac	rs121913157
Gnomad	rs121913157
Varsome	rs121913157
LitVar	rs121913157
Map	rs121913157
PheGenI	rs121913157
Biobank	rs121913157
1000 genomes	rs121913157
hgdp	rs121913157
ensembl	rs121913157
geneview	rs121913157
scholar	rs121913157
google	rs121913157
pharmgkb	rs121913157
gwascentral	rs121913157
openSNP	rs121913157
23andMe	rs121913157
SNPshot	rs121913157
SNPdbe	rs121913157
MSV3d	rs121913157
GWAS Ctlg	rs121913157

Max Magnitude

0

OMIM	147670
Desc
Variant	0031
Related	also

ClinVar
Risk	rs121913157(A;A)
Alt	rs121913157(A;A)
Reference	Rs121913157(G;G)
Significance	Pathogenic
Disease	Insulin resistance
Variation	info
Gene	INSR
CLNDBN	Insulin resistance
Reversed	1
HGVS	NC_000019.9:g.7120750C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015824.25,