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rs1057516863

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057516863(G;G)
Make rs1057516863(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position19649126
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs1057516863
dbSNP (old)rs1057516863
ClinGenrs1057516863
ebirs1057516863
HLIrs1057516863
Exacrs1057516863
Gnomadrs1057516863
Varsomers1057516863
Maprs1057516863
PheGenIrs1057516863
Biobankrs1057516863
1000 genomesrs1057516863
hgdprs1057516863
ensemblrs1057516863
gopubmedrs1057516863
geneviewrs1057516863
scholarrs1057516863
googlers1057516863
pharmgkbrs1057516863
gwascentralrs1057516863
openSNPrs1057516863
23andMers1057516863
23andMe allrs1057516863
SNPshotrs1057516863
SNPdbers1057516863
MSV3drs1057516863
GWAS Ctlgrs1057516863
Max Magnitude0
ClinVar
Risk rs1057516863(G;G)
Alt rs1057516863(G;G)
Reference Rs1057516863(T;T)
Significance Probable-Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19552439T>G
CLNSRC
CLNACC RCV000411762.1,