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rs118204429

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118204429(C;T)
Make rs118204429(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position101429901
GeneALDOB
is asnp
is mentioned by
dbSNPrs118204429
ebirs118204429
HLIrs118204429
Exacrs118204429
Varsomers118204429
Maprs118204429
PheGenIrs118204429
hapmaprs118204429
1000 genomesrs118204429
hgdprs118204429
ensemblrs118204429
gopubmedrs118204429
geneviewrs118204429
scholarrs118204429
googlers118204429
pharmgkbrs118204429
gwascentralrs118204429
openSNPrs118204429
23andMers118204429
23andMe allrs118204429
SNP Nexus

SNPshotrs118204429
SNPdbers118204429
MSV3drs118204429
GWAS Ctlgrs118204429
Max Magnitude0
OMIM612724
Desc
Variant0009
Relatedalso
ClinVar
Risk rs118204429(T;T)
Alt rs118204429(T;T)
Reference rs118204429(C;C)
Significance Other
Disease Hereditary fructosuria
Variation info
Gene ALDOB
CLNDBN Hereditary fructosuria
Reversed 1
HGVS NC_000009.11:g.104192183G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000501.5,