Have questions? Visit https://www.reddit.com/r/SNPedia

rs35882952

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35882952(G;T)
Make rs35882952(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position22863060
GeneEPHB2, MIR4253
is asnp
is mentioned by
dbSNPrs35882952
ebirs35882952
HLIrs35882952
Exacrs35882952
Varsomers35882952
Maprs35882952
PheGenIrs35882952
hapmaprs35882952
1000 genomesrs35882952
hgdprs35882952
ensemblrs35882952
gopubmedrs35882952
geneviewrs35882952
scholarrs35882952
googlers35882952
pharmgkbrs35882952
gwascentralrs35882952
openSNPrs35882952
23andMers35882952
23andMe allrs35882952
SNP Nexus

SNPshotrs35882952
SNPdbers35882952
MSV3drs35882952
GWAS Ctlgrs35882952
GMAF0.0004591
Max Magnitude0
OMIM600997
Desc
Variant0002
Relatedalso


ClinVar
Risk rs35882952(C,T;C,T)
Alt rs35882952(C,T;C,T)
Reference rs35882952(G;G)
Significance Pathogenic
Disease Prostate cancer/brain cancer susceptibility
Variation info
Gene EPHB2 MIR4253
CLNDBN Prostate cancer/brain cancer susceptibility
Reversed 0
HGVS NC_000001.10:g.23189553G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009059.5,



GET Evidence
EPHB2-A279S
aa_change Ala279Ser
aa_change_short A279S
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.00585611
summary