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rs1085307988

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome17
Position8081143
GeneALOX12B, LOC107985075
is asnp
is mentioned by
dbSNPrs1085307988
dbSNP (old)rs1085307988
ClinGenrs1085307988
ebirs1085307988
HLIrs1085307988
Exacrs1085307988
Gnomadrs1085307988
Varsomers1085307988
Maprs1085307988
PheGenIrs1085307988
Biobankrs1085307988
1000 genomesrs1085307988
hgdprs1085307988
ensemblrs1085307988
gopubmedrs1085307988
geneviewrs1085307988
scholarrs1085307988
googlers1085307988
pharmgkbrs1085307988
gwascentralrs1085307988
openSNPrs1085307988
23andMers1085307988
23andMe allrs1085307988
SNPshotrs1085307988
SNPdbers1085307988
MSV3drs1085307988
GWAS Ctlgrs1085307988
Max Magnitude0
ClinVar
Risk rs1085307988(G;G)
Alt rs1085307988(G;G)
Reference Rs1085307988(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALOX12B
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7984461T>C
CLNSRC
CLNACC RCV000489870.1,