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rs863224950

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224950(A;A)
Make rs863224950(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161983907
GeneOLFML2B
is asnp
is mentioned by
dbSNPrs863224950
ebirs863224950
HLIrs863224950
Exacrs863224950
Varsomers863224950
Maprs863224950
PheGenIrs863224950
hapmaprs863224950
1000 genomesrs863224950
hgdprs863224950
ensemblrs863224950
gopubmedrs863224950
geneviewrs863224950
scholarrs863224950
googlers863224950
pharmgkbrs863224950
gwascentralrs863224950
openSNPrs863224950
23andMers863224950
23andMe allrs863224950
SNP Nexus

SNPshotrs863224950
SNPdbers863224950
MSV3drs863224950
GWAS Ctlgrs863224950
Max Magnitude0
ClinVar
Risk rs863224950(A;A)
Alt rs863224950(A;A)
Reference rs863224950(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OLFML2B
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.161953697C>T
CLNSRC München/ Helmholtz Zentrum München
CLNACC RCV000201143.1,