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rs756430892

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756430892(C;T)
Make rs756430892(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161984875
GeneOLFML2B
is asnp
is mentioned by
dbSNPrs756430892
ebirs756430892
HLIrs756430892
Exacrs756430892
Varsomers756430892
Maprs756430892
PheGenIrs756430892
hapmaprs756430892
1000 genomesrs756430892
hgdprs756430892
ensemblrs756430892
gopubmedrs756430892
geneviewrs756430892
scholarrs756430892
googlers756430892
pharmgkbrs756430892
gwascentralrs756430892
openSNPrs756430892
23andMers756430892
23andMe allrs756430892
SNP Nexus

SNPshotrs756430892
SNPdbers756430892
MSV3drs756430892
GWAS Ctlgrs756430892
Max Magnitude0
ClinVar
Risk rs756430892(A,T;A,T)
Alt rs756430892(A,T;A,T)
Reference rs756430892(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OLFML2B
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.161954665C>T
CLNSRC München/ Helmholtz Zentrum München
CLNACC RCV000201057.1,