rs121913146

Orientation

minus

Stabilized

minus

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

Make rs121913146(A;A)

Make rs121913146(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

7267518

Gene

INSR

is a	snp
is	mentioned by
dbSNP	rs121913146
dbSNP (classic)	rs121913146
ClinGen	rs121913146
ebi	rs121913146
HLI	rs121913146
Exac	rs121913146
Gnomad	rs121913146
Varsome	rs121913146
LitVar	rs121913146
Map	rs121913146
PheGenI	rs121913146
Biobank	rs121913146
1000 genomes	rs121913146
hgdp	rs121913146
ensembl	rs121913146
geneview	rs121913146
scholar	rs121913146
google	rs121913146
pharmgkb	rs121913146
gwascentral	rs121913146
openSNP	rs121913146
23andMe	rs121913146
SNPshot	rs121913146
SNPdbe	rs121913146
MSV3d	rs121913146
GWAS Ctlg	rs121913146

Max Magnitude

0

OMIM	147670
Desc
Variant	0015
Related	also

ClinVar
Risk	rs121913146(A;A)
Alt	rs121913146(A;A)
Reference	Rs121913146(G;G)
Significance	Pathogenic
Disease	Insulin-resistant diabetes mellitus AND acanthosis nigricans
Variation	info
Gene	INSR
CLNDBN	Insulin-resistant diabetes mellitus AND acanthosis nigricans
Reversed	1
HGVS	NC_000019.9:g.7267529C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015809.29,