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rs369586696

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs369586696(A;G)
Make rs369586696(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position101421877
GeneALDOB
is asnp
is mentioned by
dbSNPrs369586696
ebirs369586696
HLIrs369586696
Exacrs369586696
Varsomers369586696
Maprs369586696
PheGenIrs369586696
hapmaprs369586696
1000 genomesrs369586696
hgdprs369586696
ensemblrs369586696
gopubmedrs369586696
geneviewrs369586696
scholarrs369586696
googlers369586696
pharmgkbrs369586696
gwascentralrs369586696
openSNPrs369586696
23andMers369586696
23andMe allrs369586696
SNP Nexus

SNPshotrs369586696
SNPdbers369586696
MSV3drs369586696
GWAS Ctlgrs369586696
Max Magnitude0
ClinVar
Risk rs369586696(G;G)
Alt rs369586696(G;G)
Reference rs369586696(A;A)
Significance Pathogenic
Disease Hereditary fructosuria
Variation info
Gene ALDOB
CLNDBN Hereditary fructosuria
Reversed 0
HGVS NC_000009.11:g.104184159A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023971.2,