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rs863224949

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224949(A;A)
Make rs863224949(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161984911
GeneOLFML2B
is asnp
is mentioned by
dbSNPrs863224949
ebirs863224949
HLIrs863224949
Exacrs863224949
Varsomers863224949
Maprs863224949
PheGenIrs863224949
hapmaprs863224949
1000 genomesrs863224949
hgdprs863224949
ensemblrs863224949
gopubmedrs863224949
geneviewrs863224949
scholarrs863224949
googlers863224949
pharmgkbrs863224949
gwascentralrs863224949
openSNPrs863224949
23andMers863224949
23andMe allrs863224949
SNP Nexus

SNPshotrs863224949
SNPdbers863224949
MSV3drs863224949
GWAS Ctlgrs863224949
Max Magnitude0
ClinVar
Risk rs863224949(A;A)
Alt rs863224949(A;A)
Reference rs863224949(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OLFML2B
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.161954701C>T
CLNSRC München/ Helmholtz Zentrum München
CLNACC RCV000201186.1,