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rs863224947

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224947(C;T)
Make rs863224947(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161998260
GeneOLFML2B
is asnp
is mentioned by
dbSNPrs863224947
ebirs863224947
HLIrs863224947
Exacrs863224947
Varsomers863224947
Maprs863224947
PheGenIrs863224947
hapmaprs863224947
1000 genomesrs863224947
hgdprs863224947
ensemblrs863224947
gopubmedrs863224947
geneviewrs863224947
scholarrs863224947
googlers863224947
pharmgkbrs863224947
gwascentralrs863224947
openSNPrs863224947
23andMers863224947
23andMe allrs863224947
SNP Nexus

SNPshotrs863224947
SNPdbers863224947
MSV3drs863224947
GWAS Ctlgrs863224947
Max Magnitude0
ClinVar
Risk rs863224947(T;T)
Alt rs863224947(T;T)
Reference rs863224947(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OLFML2B
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.161968050G>A
CLNSRC München/ Helmholtz Zentrum München
CLNACC RCV000201193.1,