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rs886039305

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs886039305(A;T)
Make rs886039305(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome17
Position19652545
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs886039305
dbSNP (classic)rs886039305
ClinGenrs886039305
ebirs886039305
HLIrs886039305
Exacrs886039305
Gnomadrs886039305
Varsomers886039305
LitVarrs886039305
Maprs886039305
PheGenIrs886039305
Biobankrs886039305
1000 genomesrs886039305
hgdprs886039305
ensemblrs886039305
geneviewrs886039305
scholarrs886039305
googlers886039305
pharmgkbrs886039305
gwascentralrs886039305
openSNPrs886039305
23andMers886039305
SNPshotrs886039305
SNPdbers886039305
MSV3drs886039305
GWAS Ctlgrs886039305
Max Magnitude0
ClinVar
Risk rs886039305(T;T)
Alt rs886039305(T;T)
Reference Rs886039305(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ALDH3A2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.19555858A>T
CLNSRC
CLNACC RCV000255004.1,