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

rs1064795242

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome7
Position44145195
GeneGCK
is asnp
is mentioned by
dbSNPrs1064795242
dbSNP (old)rs1064795242
ClinGenrs1064795242
ebirs1064795242
HLIrs1064795242
Exacrs1064795242
Gnomadrs1064795242
Varsomers1064795242
Maprs1064795242
PheGenIrs1064795242
Biobankrs1064795242
1000 genomesrs1064795242
hgdprs1064795242
ensemblrs1064795242
gopubmedrs1064795242
geneviewrs1064795242
scholarrs1064795242
googlers1064795242
pharmgkbrs1064795242
gwascentralrs1064795242
openSNPrs1064795242
23andMers1064795242
23andMe allrs1064795242
SNPshotrs1064795242
SNPdbers1064795242
MSV3drs1064795242
GWAS Ctlgrs1064795242
Max Magnitude0
ClinVar
Risk rs1064795242(-;-)
Alt rs1064795242(-;-)
Reference Rs1064795242(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GCK
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.44184794delG
CLNSRC
CLNACC RCV000481054.1,