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rs121912582

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912582(C;T)
Make rs121912582(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position22907980
GeneEPHB2
is asnp
is mentioned by
dbSNPrs121912582
ebirs121912582
HLIrs121912582
Exacrs121912582
Varsomers121912582
Maprs121912582
PheGenIrs121912582
hapmaprs121912582
1000 genomesrs121912582
hgdprs121912582
ensemblrs121912582
gopubmedrs121912582
geneviewrs121912582
scholarrs121912582
googlers121912582
pharmgkbrs121912582
gwascentralrs121912582
openSNPrs121912582
23andMers121912582
23andMe allrs121912582
SNP Nexus

SNPshotrs121912582
SNPdbers121912582
MSV3drs121912582
GWAS Ctlgrs121912582
Max Magnitude0
OMIM600997
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121912582(T;T)
Alt rs121912582(T;T)
Reference rs121912582(C;C)
Significance Pathogenic
Disease Prostate cancer/brain cancer susceptibility
Variation info
Gene EPHB2
CLNDBN Prostate cancer/brain cancer susceptibility
Reversed 0
HGVS NC_000001.10:g.23234473C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009058.6,