rs121913154

Orientation

minus

Stabilized

minus

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

Make rs121913154(A;A)

Make rs121913154(A;C)

Reference

GRCh38 38.1/141

Chromosome

19

Position

7122658

Gene

INSR

is a	snp
is	mentioned by
dbSNP	rs121913154
dbSNP (classic)	rs121913154
ClinGen	rs121913154
ebi	rs121913154
HLI	rs121913154
Exac	rs121913154
Gnomad	rs121913154
Varsome	rs121913154
LitVar	rs121913154
Map	rs121913154
PheGenI	rs121913154
Biobank	rs121913154
1000 genomes	rs121913154
hgdp	rs121913154
ensembl	rs121913154
geneview	rs121913154
scholar	rs121913154
google	rs121913154
pharmgkb	rs121913154
gwascentral	rs121913154
openSNP	rs121913154
23andMe	rs121913154
SNPshot	rs121913154
SNPdbe	rs121913154
MSV3d	rs121913154
GWAS Ctlg	rs121913154

Max Magnitude

0

OMIM	147670
Desc
Variant	0026
Related	also

ClinVar
Risk	rs121913154(A;A)
Alt	rs121913154(A;A)
Reference	Rs121913154(C;C)
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.7122669G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015819.29,