rs121913142

Orientation

minus

Stabilized

minus

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

Make rs121913142(G;G)

Make rs121913142(G;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

7172333

Gene

INSR

is a	snp
is	mentioned by
dbSNP	rs121913142
dbSNP (classic)	rs121913142
ClinGen	rs121913142
ebi	rs121913142
HLI	rs121913142
Exac	rs121913142
Gnomad	rs121913142
Varsome	rs121913142
LitVar	rs121913142
Map	rs121913142
PheGenI	rs121913142
Biobank	rs121913142
1000 genomes	rs121913142
hgdp	rs121913142
ensembl	rs121913142
geneview	rs121913142
scholar	rs121913142
google	rs121913142
pharmgkb	rs121913142
gwascentral	rs121913142
openSNP	rs121913142
23andMe	rs121913142
SNPshot	rs121913142
SNPdbe	rs121913142
MSV3d	rs121913142
GWAS Ctlg	rs121913142

Max Magnitude

0

OMIM	147670
Desc
Variant	0011
Related	also

ClinVar
Risk	rs121913142(G;G)
Alt	rs121913142(G;G)
Reference	Rs121913142(T;T)
Significance	Pathogenic
Disease	Diabetes mellitus
Variation	info
Gene	INSR
CLNDBN	Diabetes mellitus, insulin-resistant
Reversed	1
HGVS	NC_000019.9:g.7172344A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015805.33,