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rs1057517278

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517278(A;A)
Make rs1057517278(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position19657863
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs1057517278
dbSNP (old)rs1057517278
ClinGenrs1057517278
ebirs1057517278
HLIrs1057517278
Exacrs1057517278
Gnomadrs1057517278
Varsomers1057517278
Maprs1057517278
PheGenIrs1057517278
Biobankrs1057517278
1000 genomesrs1057517278
hgdprs1057517278
ensemblrs1057517278
gopubmedrs1057517278
geneviewrs1057517278
scholarrs1057517278
googlers1057517278
pharmgkbrs1057517278
gwascentralrs1057517278
openSNPrs1057517278
23andMers1057517278
23andMe allrs1057517278
SNPshotrs1057517278
SNPdbers1057517278
MSV3drs1057517278
GWAS Ctlgrs1057517278
Max Magnitude0
ClinVar
Risk rs1057517278(A;A)
Alt rs1057517278(A;A)
Reference Rs1057517278(G;G)
Significance Probable-Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19561176G>A
CLNSRC
CLNACC RCV000409063.1,