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rs146175795

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs146175795(A;A)
Make rs146175795(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position27498276
GeneGCKR
is asnp
is mentioned by
dbSNPrs146175795
dbSNP (old)rs146175795
ClinGenrs146175795
ebirs146175795
HLIrs146175795
Exacrs146175795
Gnomadrs146175795
Varsomers146175795
LitVarrs146175795
Maprs146175795
PheGenIrs146175795
Biobankrs146175795
1000 genomesrs146175795
hgdprs146175795
ensemblrs146175795
gopubmedrs146175795
geneviewrs146175795
scholarrs146175795
googlers146175795
pharmgkbrs146175795
gwascentralrs146175795
openSNPrs146175795
23andMers146175795
23andMe allrs146175795
SNPshotrs146175795
SNPdbers146175795
MSV3drs146175795
GWAS Ctlgrs146175795
Max Magnitude0
ClinVar
Risk rs146175795(A;A) rs146175795(T;T)
Alt rs146175795(A;A) rs146175795(T;T)
Reference Rs146175795(G;G)
Significance Probable-Pathogenic
Disease Fasting plasma glucose level quantitative trait locus 5
Variation info
Gene GCKR
CLNDBN Fasting plasma glucose level quantitative trait locus 5
Reversed 0
HGVS NC_000002.11:g.27721143G>A
CLNSRC
CLNACC RCV000490466.1,