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rs202210810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202210810(A;A)
Make rs202210810(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position101427534
GeneALDOB
is asnp
is mentioned by
dbSNPrs202210810
dbSNP (classic)rs202210810
ClinGenrs202210810
ebirs202210810
HLIrs202210810
Exacrs202210810
Gnomadrs202210810
Varsomers202210810
LitVarrs202210810
Maprs202210810
PheGenIrs202210810
Biobankrs202210810
1000 genomesrs202210810
hgdprs202210810
ensemblrs202210810
geneviewrs202210810
scholarrs202210810
googlers202210810
pharmgkbrs202210810
gwascentralrs202210810
openSNPrs202210810
23andMers202210810
SNPshotrs202210810
SNPdbers202210810
MSV3drs202210810
GWAS Ctlgrs202210810
Max Magnitude0
ClinVar
Risk rs202210810(A;A)
Alt rs202210810(A;A)
Reference Rs202210810(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALDOB
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.104189816G>A
CLNSRC
CLNACC RCV000420841.1,