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

rs1060502465

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502465(-;-)
Make rs1060502465(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32326504
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502465
dbSNP (old)rs1060502465
ClinGenrs1060502465
ebirs1060502465
HLIrs1060502465
Exacrs1060502465
Gnomadrs1060502465
Varsomers1060502465
Maprs1060502465
PheGenIrs1060502465
Biobankrs1060502465
1000 genomesrs1060502465
hgdprs1060502465
ensemblrs1060502465
gopubmedrs1060502465
geneviewrs1060502465
scholarrs1060502465
googlers1060502465
pharmgkbrs1060502465
gwascentralrs1060502465
openSNPrs1060502465
23andMers1060502465
23andMe allrs1060502465
SNPshotrs1060502465
SNPdbers1060502465
MSV3drs1060502465
GWAS Ctlgrs1060502465
Max Magnitude0
ClinVar
Risk rs1060502465(-;-)
Alt rs1060502465(-;-)
Reference Rs1060502465(T;T)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32900641delT
CLNSRC
CLNACC RCV000476820.1,