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rs1057518381

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518381(A;A)
Make rs1057518381(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position8080778
GeneALOX12B, LOC107985075
is asnp
is mentioned by
dbSNPrs1057518381
dbSNP (old)rs1057518381
ClinGenrs1057518381
ebirs1057518381
HLIrs1057518381
Exacrs1057518381
Gnomadrs1057518381
Varsomers1057518381
Maprs1057518381
PheGenIrs1057518381
Biobankrs1057518381
1000 genomesrs1057518381
hgdprs1057518381
ensemblrs1057518381
gopubmedrs1057518381
geneviewrs1057518381
scholarrs1057518381
googlers1057518381
pharmgkbrs1057518381
gwascentralrs1057518381
openSNPrs1057518381
23andMers1057518381
23andMe allrs1057518381
SNPshotrs1057518381
SNPdbers1057518381
MSV3drs1057518381
GWAS Ctlgrs1057518381
Max Magnitude0
ClinVar
Risk rs1057518381(A;A)
Alt rs1057518381(A;A)
Reference Rs1057518381(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ALOX12B
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7984096C>T
CLNSRC
CLNACC RCV000413742.1,