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rs138121153

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs138121153(A;A)
Make rs138121153(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position101428468
GeneALDOB
is asnp
is mentioned by
dbSNPrs138121153
dbSNP (old)rs138121153
ClinGenrs138121153
ebirs138121153
HLIrs138121153
Exacrs138121153
Gnomadrs138121153
Varsomers138121153
Maprs138121153
PheGenIrs138121153
Biobankrs138121153
1000 genomesrs138121153
hgdprs138121153
ensemblrs138121153
gopubmedrs138121153
geneviewrs138121153
scholarrs138121153
googlers138121153
pharmgkbrs138121153
gwascentralrs138121153
openSNPrs138121153
23andMers138121153
23andMe allrs138121153
SNPshotrs138121153
SNPdbers138121153
MSV3drs138121153
GWAS Ctlgrs138121153
Max Magnitude0
ClinVar
Risk rs138121153(A;A) rs138121153(T;T)
Alt rs138121153(A;A) rs138121153(T;T)
Reference Rs138121153(C;C)
Significance Probable-Pathogenic
Disease Hereditary fructosuria
Variation info
Gene ALDOB
CLNDBN Hereditary fructosuria
Reversed 0
HGVS NC_000009.11:g.104190750C>T
CLNSRC
CLNACC RCV000409543.1,