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rs1036733598

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position19664947
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs1036733598
dbSNP (old)rs1036733598
ClinGenrs1036733598
ebirs1036733598
HLIrs1036733598
Exacrs1036733598
Gnomadrs1036733598
Varsomers1036733598
Maprs1036733598
PheGenIrs1036733598
Biobankrs1036733598
1000 genomesrs1036733598
hgdprs1036733598
ensemblrs1036733598
gopubmedrs1036733598
geneviewrs1036733598
scholarrs1036733598
googlers1036733598
pharmgkbrs1036733598
gwascentralrs1036733598
openSNPrs1036733598
23andMers1036733598
23andMe allrs1036733598
SNPshotrs1036733598
SNPdbers1036733598
MSV3drs1036733598
GWAS Ctlgrs1036733598
Max Magnitude0
ClinVar
Risk rs1036733598(C;C)
Alt rs1036733598(C;C)
Reference Rs1036733598(G;G)
Significance Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19568260G>C; NC_000017.10:g.19568260G>T
CLNSRC
CLNACC RCV000411369.1, RCV000410648.1,