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rs1057516742

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057516742(A;G)
Make rs1057516742(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position19664946
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs1057516742
dbSNP (old)rs1057516742
ClinGenrs1057516742
ebirs1057516742
HLIrs1057516742
Exacrs1057516742
Gnomadrs1057516742
Varsomers1057516742
Maprs1057516742
PheGenIrs1057516742
Biobankrs1057516742
1000 genomesrs1057516742
hgdprs1057516742
ensemblrs1057516742
gopubmedrs1057516742
geneviewrs1057516742
scholarrs1057516742
googlers1057516742
pharmgkbrs1057516742
gwascentralrs1057516742
openSNPrs1057516742
23andMers1057516742
23andMe allrs1057516742
SNPshotrs1057516742
SNPdbers1057516742
MSV3drs1057516742
GWAS Ctlgrs1057516742
Max Magnitude0
ClinVar
Risk rs1057516742(G;G)
Alt rs1057516742(G;G)
Reference Rs1057516742(A;A)
Significance Probable-Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19568259A>G
CLNSRC
CLNACC RCV000411031.1,