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rs28936395

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28936395(A;A)
Make rs28936395(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position22906853
GeneEPHB2
is asnp
is mentioned by
dbSNPrs28936395
ebirs28936395
HLIrs28936395
Exacrs28936395
Varsomers28936395
Maprs28936395
PheGenIrs28936395
hapmaprs28936395
1000 genomesrs28936395
hgdprs28936395
ensemblrs28936395
gopubmedrs28936395
geneviewrs28936395
scholarrs28936395
googlers28936395
pharmgkbrs28936395
gwascentralrs28936395
openSNPrs28936395
23andMers28936395
23andMe allrs28936395
SNP Nexus

SNPshotrs28936395
SNPdbers28936395
MSV3drs28936395
GWAS Ctlgrs28936395
GMAF0.002296
Max Magnitude0
OMIM600997
DescPROSTATE CANCER, PROGRESSION AND METASTASIS OF
Variant0003
Relatedalso


ClinVar
Risk rs28936395(A;A)
Alt rs28936395(A;A)
Reference rs28936395(G;G)
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.23233346G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009060.5,