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rs1064793998

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome7
Position44153325
GeneGCK
is asnp
is mentioned by
dbSNPrs1064793998
dbSNP (old)rs1064793998
ClinGenrs1064793998
ebirs1064793998
HLIrs1064793998
Exacrs1064793998
Gnomadrs1064793998
Varsomers1064793998
Maprs1064793998
PheGenIrs1064793998
Biobankrs1064793998
1000 genomesrs1064793998
hgdprs1064793998
ensemblrs1064793998
gopubmedrs1064793998
geneviewrs1064793998
scholarrs1064793998
googlers1064793998
pharmgkbrs1064793998
gwascentralrs1064793998
openSNPrs1064793998
23andMers1064793998
23andMe allrs1064793998
SNPshotrs1064793998
SNPdbers1064793998
MSV3drs1064793998
GWAS Ctlgrs1064793998
Max Magnitude0
ClinVar
Risk rs1064793998(A;A)
Alt rs1064793998(A;A)
Reference Rs1064793998(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GCK
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.44192924C>T
CLNSRC
CLNACC RCV000481874.1,