Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057516379

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057516379(A;A)
Make rs1057516379(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position101429753
GeneALDOB
is asnp
is mentioned by
dbSNPrs1057516379
dbSNP (classic)rs1057516379
ClinGenrs1057516379
ebirs1057516379
HLIrs1057516379
Exacrs1057516379
Gnomadrs1057516379
Varsomers1057516379
LitVarrs1057516379
Maprs1057516379
PheGenIrs1057516379
Biobankrs1057516379
1000 genomesrs1057516379
hgdprs1057516379
ensemblrs1057516379
geneviewrs1057516379
scholarrs1057516379
googlers1057516379
pharmgkbrs1057516379
gwascentralrs1057516379
openSNPrs1057516379
23andMers1057516379
SNPshotrs1057516379
SNPdbers1057516379
MSV3drs1057516379
GWAS Ctlgrs1057516379
Max Magnitude0
ClinVar
Risk rs1057516379(A;A)
Alt rs1057516379(A;A)
Reference Rs1057516379(T;T)
Significance Probable-Pathogenic
Disease Hereditary fructosuria
Variation info
Gene ALDOB
CLNDBN Hereditary fructosuria
Reversed 1
HGVS NC_000009.11:g.104192035A>T
CLNSRC
CLNACC RCV000409519.1,