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rs863224948

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224948(G;T)
Make rs863224948(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161997993
GeneOLFML2B
is asnp
is mentioned by
dbSNPrs863224948
ebirs863224948
HLIrs863224948
Exacrs863224948
Varsomers863224948
Maprs863224948
PheGenIrs863224948
hapmaprs863224948
1000 genomesrs863224948
hgdprs863224948
ensemblrs863224948
gopubmedrs863224948
geneviewrs863224948
scholarrs863224948
googlers863224948
pharmgkbrs863224948
gwascentralrs863224948
openSNPrs863224948
23andMers863224948
23andMe allrs863224948
SNP Nexus

SNPshotrs863224948
SNPdbers863224948
MSV3drs863224948
GWAS Ctlgrs863224948
Max Magnitude0
ClinVar
Risk rs863224948(T;T)
Alt rs863224948(T;T)
Reference rs863224948(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OLFML2B
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.161967783C>A
CLNSRC München/ Helmholtz Zentrum München
CLNACC RCV000201124.1,