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rs41281039

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41281039(A;A)
Make rs41281039(A;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position101429943
GeneALDOB
is asnp
is mentioned by
dbSNPrs41281039
ebirs41281039
HLIrs41281039
Exacrs41281039
Varsomers41281039
Maprs41281039
PheGenIrs41281039
hapmaprs41281039
1000 genomesrs41281039
hgdprs41281039
ensemblrs41281039
gopubmedrs41281039
geneviewrs41281039
scholarrs41281039
googlers41281039
pharmgkbrs41281039
gwascentralrs41281039
openSNPrs41281039
23andMers41281039
23andMe allrs41281039
SNP Nexus

SNPshotrs41281039
SNPdbers41281039
MSV3drs41281039
GWAS Ctlgrs41281039
Max Magnitude0
ClinVar
Risk rs41281039(A;A)
Alt rs41281039(A;A)
Reference rs41281039(T;T)
Significance Pathogenic
Disease Hereditary fructosuria
Variation info
Gene ALDOB
CLNDBN Hereditary fructosuria
Reversed 0
HGVS NC_000009.11:g.104192225T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023970.2,