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rs387906255

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906255(-;-)
Make rs387906255(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position19661137
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs387906255
ebirs387906255
HLIrs387906255
Exacrs387906255
Varsomers387906255
Maprs387906255
PheGenIrs387906255
hapmaprs387906255
1000 genomesrs387906255
hgdprs387906255
ensemblrs387906255
gopubmedrs387906255
geneviewrs387906255
scholarrs387906255
googlers387906255
pharmgkbrs387906255
gwascentralrs387906255
openSNPrs387906255
23andMers387906255
23andMe allrs387906255
SNP Nexus

SNPshotrs387906255
SNPdbers387906255
MSV3drs387906255
GWAS Ctlgrs387906255
Max Magnitude0
ClinVar
Risk rs387906255(;)
Alt rs387906255(;)
Reference rs387906255(G;G)
Significance Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19564450delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000001704.3,