Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057516788

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs1057516788(-;-)
Make rs1057516788(-;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position19661152
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs1057516788
dbSNP (old)rs1057516788
ClinGenrs1057516788
ebirs1057516788
HLIrs1057516788
Exacrs1057516788
Gnomadrs1057516788
Varsomers1057516788
Maprs1057516788
PheGenIrs1057516788
Biobankrs1057516788
1000 genomesrs1057516788
hgdprs1057516788
ensemblrs1057516788
gopubmedrs1057516788
geneviewrs1057516788
scholarrs1057516788
googlers1057516788
pharmgkbrs1057516788
gwascentralrs1057516788
openSNPrs1057516788
23andMers1057516788
23andMe allrs1057516788
SNPshotrs1057516788
SNPdbers1057516788
MSV3drs1057516788
GWAS Ctlgrs1057516788
Max Magnitude0
ClinVar
Risk rs1057516788(-;-)
Alt rs1057516788(-;-)
Reference Rs1057516788(AG;AG)
Significance Probable-Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19564465_19564466delAG
CLNSRC
CLNACC RCV000411692.1,