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rs118204426

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118204426(A;A)
Make rs118204426(A;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position101425532
GeneALDOB
is asnp
is mentioned by
dbSNPrs118204426
ebirs118204426
HLIrs118204426
Exacrs118204426
Varsomers118204426
Maprs118204426
PheGenIrs118204426
hapmaprs118204426
1000 genomesrs118204426
hgdprs118204426
ensemblrs118204426
gopubmedrs118204426
geneviewrs118204426
scholarrs118204426
googlers118204426
pharmgkbrs118204426
gwascentralrs118204426
openSNPrs118204426
23andMers118204426
23andMe allrs118204426
SNP Nexus

SNPshotrs118204426
SNPdbers118204426
MSV3drs118204426
GWAS Ctlgrs118204426
Max Magnitude0
OMIM612724
Desc
Variant0005
Relatedalso
ClinVar
Risk rs118204426(A;A)
Alt rs118204426(A;A)
Reference rs118204426(C;C)
Significance Pathogenic
Disease Hereditary fructosuria
Variation info
Gene ALDOB
CLNDBN Hereditary fructosuria
Reversed 1
HGVS NC_000009.11:g.104187814G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000497.2,