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rs1057517091

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517091(-;-)
Make rs1057517091(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position101426633
GeneALDOB
is asnp
is mentioned by
dbSNPrs1057517091
dbSNP (old)rs1057517091
ClinGenrs1057517091
ebirs1057517091
HLIrs1057517091
Exacrs1057517091
Gnomadrs1057517091
Varsomers1057517091
Maprs1057517091
PheGenIrs1057517091
Biobankrs1057517091
1000 genomesrs1057517091
hgdprs1057517091
ensemblrs1057517091
gopubmedrs1057517091
geneviewrs1057517091
scholarrs1057517091
googlers1057517091
pharmgkbrs1057517091
gwascentralrs1057517091
openSNPrs1057517091
23andMers1057517091
23andMe allrs1057517091
SNPshotrs1057517091
SNPdbers1057517091
MSV3drs1057517091
GWAS Ctlgrs1057517091
Max Magnitude0
ClinVar
Risk rs1057517091(-;-)
Alt rs1057517091(-;-)
Reference Rs1057517091(A;A)
Significance Probable-Pathogenic
Disease Hereditary fructosuria
Variation info
Gene ALDOB
CLNDBN Hereditary fructosuria
Reversed 1
HGVS NC_000009.11:g.104188915delT
CLNSRC
CLNACC RCV000410076.1,