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rs184770596

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs184770596(C;G)
Make rs184770596(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position73938978
GeneDGUOK
is asnp
is mentioned by
dbSNPrs184770596
ebirs184770596
HLIrs184770596
Exacrs184770596
Varsomers184770596
Maprs184770596
PheGenIrs184770596
hapmaprs184770596
1000 genomesrs184770596
hgdprs184770596
ensemblrs184770596
gopubmedrs184770596
geneviewrs184770596
scholarrs184770596
googlers184770596
pharmgkbrs184770596
gwascentralrs184770596
openSNPrs184770596
23andMers184770596
23andMe allrs184770596
SNP Nexus

SNPshotrs184770596
SNPdbers184770596
MSV3drs184770596
GWAS Ctlgrs184770596
Max Magnitude0
ClinVar
Risk rs184770596(G;G)
Alt rs184770596(G;G)
Reference rs184770596(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene DGUOK
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000002.11:g.74166105C>G
CLNSRC
CLNACC RCV000190772.1,