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rs142806829

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs142806829(A;A)
Make rs142806829(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161998241
GeneOLFML2B
is asnp
is mentioned by
dbSNPrs142806829
ebirs142806829
HLIrs142806829
Exacrs142806829
Varsomers142806829
Maprs142806829
PheGenIrs142806829
hapmaprs142806829
1000 genomesrs142806829
hgdprs142806829
ensemblrs142806829
gopubmedrs142806829
geneviewrs142806829
scholarrs142806829
googlers142806829
pharmgkbrs142806829
gwascentralrs142806829
openSNPrs142806829
23andMers142806829
23andMe allrs142806829
SNP Nexus

SNPshotrs142806829
SNPdbers142806829
MSV3drs142806829
GWAS Ctlgrs142806829
Max Magnitude0
ClinVar
Risk rs142806829(A,T;A,T)
Alt rs142806829(A,T;A,T)
Reference rs142806829(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OLFML2B
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.161968031C>T
CLNSRC München/ Helmholtz Zentrum München
CLNACC RCV000201067.1,