Have questions? Visit https://www.reddit.com/r/SNPedia

rs1801483

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1801483(A;A)
Make rs1801483(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position81809839
GeneGCGR
is asnp
is mentioned by
dbSNPrs1801483
ebirs1801483
HLIrs1801483
Exacrs1801483
Varsomers1801483
Maprs1801483
PheGenIrs1801483
hapmaprs1801483
1000 genomesrs1801483
hgdprs1801483
ensemblrs1801483
gopubmedrs1801483
geneviewrs1801483
scholarrs1801483
googlers1801483
pharmgkbrs1801483
gwascentralrs1801483
openSNPrs1801483
23andMers1801483
23andMe allrs1801483
SNP Nexus

SNPshotrs1801483
SNPdbers1801483
MSV3drs1801483
GWAS Ctlgrs1801483
GMAF0.004591
Max Magnitude0
OMIM138033
Desc
Variant0001
Relatedalso
ClinVar
Risk rs1801483(A;A)
Alt rs1801483(A;A)
Reference rs1801483(G;G)
Significance Pathogenic
Disease Diabetes mellitus type 2
Variation info
Gene GCGR
CLNDBN Diabetes mellitus type 2
Reversed 0
HGVS NC_000017.10:g.79767715G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017542.27,