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rs185436876

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs185436876(C;T)
Make rs185436876(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161984849
GeneOLFML2B
is asnp
is mentioned by
dbSNPrs185436876
ebirs185436876
HLIrs185436876
Exacrs185436876
Varsomers185436876
Maprs185436876
PheGenIrs185436876
hapmaprs185436876
1000 genomesrs185436876
hgdprs185436876
ensemblrs185436876
gopubmedrs185436876
geneviewrs185436876
scholarrs185436876
googlers185436876
pharmgkbrs185436876
gwascentralrs185436876
openSNPrs185436876
23andMers185436876
23andMe allrs185436876
SNP Nexus

SNPshotrs185436876
SNPdbers185436876
MSV3drs185436876
GWAS Ctlgrs185436876
Max Magnitude0
ClinVar
Risk rs185436876(T;T)
Alt rs185436876(T;T)
Reference rs185436876(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OLFML2B
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.161954639C>T
CLNSRC München/ Helmholtz Zentrum München
CLNACC RCV000201204.1,