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rs1057517190

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517190(-;A)
Make rs1057517190(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position19657833
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs1057517190
dbSNP (old)rs1057517190
ClinGenrs1057517190
ebirs1057517190
HLIrs1057517190
Exacrs1057517190
Gnomadrs1057517190
Varsomers1057517190
Maprs1057517190
PheGenIrs1057517190
Biobankrs1057517190
1000 genomesrs1057517190
hgdprs1057517190
ensemblrs1057517190
gopubmedrs1057517190
geneviewrs1057517190
scholarrs1057517190
googlers1057517190
pharmgkbrs1057517190
gwascentralrs1057517190
openSNPrs1057517190
23andMers1057517190
23andMe allrs1057517190
SNPshotrs1057517190
SNPdbers1057517190
MSV3drs1057517190
GWAS Ctlgrs1057517190
Max Magnitude0
ClinVar
Risk rs1057517190(A;A)
Alt rs1057517190(A;A)
Reference Rs1057517190(-;-)
Significance Probable-Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19561146dupA
CLNSRC
CLNACC RCV000412314.1,