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rs1057516386

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057516386(-;-)
Make rs1057516386(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position19651624
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs1057516386
dbSNP (old)rs1057516386
ClinGenrs1057516386
ebirs1057516386
HLIrs1057516386
Exacrs1057516386
Gnomadrs1057516386
Varsomers1057516386
Maprs1057516386
PheGenIrs1057516386
Biobankrs1057516386
1000 genomesrs1057516386
hgdprs1057516386
ensemblrs1057516386
gopubmedrs1057516386
geneviewrs1057516386
scholarrs1057516386
googlers1057516386
pharmgkbrs1057516386
gwascentralrs1057516386
openSNPrs1057516386
23andMers1057516386
23andMe allrs1057516386
SNPshotrs1057516386
SNPdbers1057516386
MSV3drs1057516386
GWAS Ctlgrs1057516386
Max Magnitude0
ClinVar
Risk rs1057516386(-;-)
Alt rs1057516386(-;-)
Reference Rs1057516386(A;A)
Significance Probable-Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19554937delA
CLNSRC
CLNACC RCV000409110.1,