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rs1057516481

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516481(-;A)
Make rs1057516481(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position19651674
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs1057516481
dbSNP (old)rs1057516481
ClinGenrs1057516481
ebirs1057516481
HLIrs1057516481
Exacrs1057516481
Gnomadrs1057516481
Varsomers1057516481
Maprs1057516481
PheGenIrs1057516481
Biobankrs1057516481
1000 genomesrs1057516481
hgdprs1057516481
ensemblrs1057516481
gopubmedrs1057516481
geneviewrs1057516481
scholarrs1057516481
googlers1057516481
pharmgkbrs1057516481
gwascentralrs1057516481
openSNPrs1057516481
23andMers1057516481
23andMe allrs1057516481
SNPshotrs1057516481
SNPdbers1057516481
MSV3drs1057516481
GWAS Ctlgrs1057516481
Max Magnitude0
ClinVar
Risk rs1057516481(A;A)
Alt rs1057516481(A;A)
Reference Rs1057516481(-;-)
Significance Probable-Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19554987dupA
CLNSRC
CLNACC RCV000412357.1,