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rs786204625

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204625(-;-)
Make rs786204625(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position19663492
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs786204625
ebirs786204625
HLIrs786204625
Exacrs786204625
Varsomers786204625
Maprs786204625
PheGenIrs786204625
hapmaprs786204625
1000 genomesrs786204625
hgdprs786204625
ensemblrs786204625
gopubmedrs786204625
geneviewrs786204625
scholarrs786204625
googlers786204625
pharmgkbrs786204625
gwascentralrs786204625
openSNPrs786204625
23andMers786204625
23andMe allrs786204625
SNP Nexus

SNPshotrs786204625
SNPdbers786204625
MSV3drs786204625
GWAS Ctlgrs786204625
Max Magnitude0
ClinVar
Risk rs786204625(;)
Alt rs786204625(;)
Reference rs786204625(A;A)
Significance Probable-Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19566805delA
CLNSRC
CLNACC RCV000169395.1,