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rs387906256

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(GA;GA) 0 common in clinvar
Make rs387906256(-;-)
Make rs387906256(-;GA)
ReferenceGRCh38 38.1/141
Chromosome17
Position19671810
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs387906256
ebirs387906256
HLIrs387906256
Exacrs387906256
Varsomers387906256
Maprs387906256
PheGenIrs387906256
hapmaprs387906256
1000 genomesrs387906256
hgdprs387906256
ensemblrs387906256
gopubmedrs387906256
geneviewrs387906256
scholarrs387906256
googlers387906256
pharmgkbrs387906256
gwascentralrs387906256
openSNPrs387906256
23andMers387906256
23andMe allrs387906256
SNP Nexus

SNPshotrs387906256
SNPdbers387906256
MSV3drs387906256
GWAS Ctlgrs387906256
Max Magnitude0
ClinVar
Risk rs387906256(;)
Alt rs387906256(;)
Reference rs387906256(AG;AG)
Significance Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19575123_19575124delGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000001708.3,