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rs78340951

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3 carrier of hereditary fructose intolerance allele
Make rs78340951(G;G)
ReferenceGRCh38 38.1/142
Chromosome9
Position101421899
GeneALDOB
is asnp
is mentioned by
dbSNPrs78340951
ebirs78340951
HLIrs78340951
Exacrs78340951
Varsomers78340951
Maprs78340951
PheGenIrs78340951
hapmaprs78340951
1000 genomesrs78340951
hgdprs78340951
ensemblrs78340951
gopubmedrs78340951
geneviewrs78340951
scholarrs78340951
googlers78340951
pharmgkbrs78340951
gwascentralrs78340951
openSNPrs78340951
23andMers78340951
23andMe allrs78340951
SNP Nexus

SNPshotrs78340951
SNPdbers78340951
MSV3drs78340951
GWAS Ctlgrs78340951
Max Magnitude3
OMIM612724
Desc
Variant0006
Relatedalso
ClinVar
Risk rs78340951(G,T;G,T)
Alt rs78340951(G,T;G,T)
Reference rs78340951(C;C)
Significance Pathogenic
Disease Hereditary fructosuria
Variation info
Gene ALDOB
CLNDBN Hereditary fructosuria
Reversed 1
HGVS NC_000009.11:g.104184181G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000498.3,