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rs1057516851

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516851(-;-)
Make rs1057516851(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position19656471
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs1057516851
dbSNP (old)rs1057516851
ClinGenrs1057516851
ebirs1057516851
HLIrs1057516851
Exacrs1057516851
Gnomadrs1057516851
Varsomers1057516851
Maprs1057516851
PheGenIrs1057516851
Biobankrs1057516851
1000 genomesrs1057516851
hgdprs1057516851
ensemblrs1057516851
gopubmedrs1057516851
geneviewrs1057516851
scholarrs1057516851
googlers1057516851
pharmgkbrs1057516851
gwascentralrs1057516851
openSNPrs1057516851
23andMers1057516851
23andMe allrs1057516851
SNPshotrs1057516851
SNPdbers1057516851
MSV3drs1057516851
GWAS Ctlgrs1057516851
Max Magnitude0
ClinVar
Risk rs1057516851(-;-)
Alt rs1057516851(-;-)
Reference Rs1057516851(G;G)
Significance Probable-Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19559784delG
CLNSRC
CLNACC RCV000409048.1,