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rs76826147

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs76826147(A;T)
Make rs76826147(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position22913757
GeneEPHB2
is asnp
is mentioned by
dbSNPrs76826147
ebirs76826147
HLIrs76826147
Exacrs76826147
Varsomers76826147
Maprs76826147
PheGenIrs76826147
hapmaprs76826147
1000 genomesrs76826147
hgdprs76826147
ensemblrs76826147
gopubmedrs76826147
geneviewrs76826147
scholarrs76826147
googlers76826147
pharmgkbrs76826147
gwascentralrs76826147
openSNPrs76826147
23andMers76826147
23andMe allrs76826147
SNP Nexus

SNPshotrs76826147
SNPdbers76826147
MSV3drs76826147
GWAS Ctlgrs76826147
GMAF0.0124
Max Magnitude0
OMIM600997
Desc
Variant0004
Relatedalso
ClinVar
Risk rs76826147(G,T;G,T)
Alt rs76826147(G,T;G,T)
Reference rs76826147(A;A)
Significance Other
Disease Prostate cancer/brain cancer susceptibility
Variation info
Gene EPHB2
CLNDBN Prostate cancer/brain cancer susceptibility
Reversed 0
HGVS NC_000001.10:g.23240250A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009061.4,