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rs104894009

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Orientationminus
Stabilizedminus
Geno Mag Summary
(C;G) 2 associated with MODY2; maturity onset of diabetes in the young (type 2)
(G;G) 0 common in clinvar


Make rs104894009(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position44146587
GeneGCK
is asnp
is mentioned by
dbSNPrs104894009
ebirs104894009
HLIrs104894009
Exacrs104894009
Varsomers104894009
Maprs104894009
PheGenIrs104894009
hapmaprs104894009
1000 genomesrs104894009
hgdprs104894009
ensemblrs104894009
gopubmedrs104894009
geneviewrs104894009
scholarrs104894009
googlers104894009
pharmgkbrs104894009
gwascentralrs104894009
openSNPrs104894009
23andMers104894009
23andMe allrs104894009
SNP Nexus

SNPshotrs104894009
SNPdbers104894009
MSV3drs104894009
GWAS Ctlgrs104894009
Max Magnitude2
OMIM138079
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894009(C;C)
Alt rs104894009(C;C)
Reference rs104894009(G;G)
Significance Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene GCK
CLNDBN Maturity-onset diabetes of the young, type 2
Reversed 1
HGVS NC_000007.13:g.44186186C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017516.28,