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

rs759874793

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs759874793(A;A)
Make rs759874793(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position19651627
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs759874793
dbSNP (classic)rs759874793
ClinGenrs759874793
ebirs759874793
HLIrs759874793
Exacrs759874793
Gnomadrs759874793
Varsomers759874793
LitVarrs759874793
Maprs759874793
PheGenIrs759874793
Biobankrs759874793
1000 genomesrs759874793
hgdprs759874793
ensemblrs759874793
geneviewrs759874793
scholarrs759874793
googlers759874793
pharmgkbrs759874793
gwascentralrs759874793
openSNPrs759874793
23andMers759874793
23andMe allrs759874793
SNPshotrs759874793
SNPdbers759874793
MSV3drs759874793
GWAS Ctlgrs759874793
Max Magnitude0
ClinVar
Risk rs759874793(A;A) rs759874793(C;C)
Alt rs759874793(A;A) rs759874793(C;C)
Reference Rs759874793(G;G)
Significance Probable-Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19554940G>A
CLNSRC
CLNACC RCV000410260.1,