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

rs104894015

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894015(A;G)
Make rs104894015(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44149798
GeneGCK
is asnp
is mentioned by
dbSNPrs104894015
ebirs104894015
HLIrs104894015
Exacrs104894015
Varsomers104894015
Maprs104894015
PheGenIrs104894015
hapmaprs104894015
1000 genomesrs104894015
hgdprs104894015
ensemblrs104894015
gopubmedrs104894015
geneviewrs104894015
scholarrs104894015
googlers104894015
pharmgkbrs104894015
gwascentralrs104894015
openSNPrs104894015
23andMers104894015
23andMe allrs104894015
SNP Nexus

SNPshotrs104894015
SNPdbers104894015
MSV3drs104894015
GWAS Ctlgrs104894015
Max Magnitude0
OMIM138079
Desc
Variant0013
Relatedalso
ClinVar
Risk rs104894015(G;G)
Alt rs104894015(G;G)
Reference rs104894015(A;A)
Significance Pathogenic
Disease Hyperinsulinemic hypoglycemia familial 3
Variation info
Gene GCK
CLNDBN Hyperinsulinemic hypoglycemia familial 3
Reversed 1
HGVS NC_000007.13:g.44189397T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017526.27,