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rs1060502466

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502466(C;C)
Make rs1060502466(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32336837
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502466
dbSNP (old)rs1060502466
ClinGenrs1060502466
ebirs1060502466
HLIrs1060502466
Exacrs1060502466
Gnomadrs1060502466
Varsomers1060502466
LitVarrs1060502466
Maprs1060502466
PheGenIrs1060502466
Biobankrs1060502466
1000 genomesrs1060502466
hgdprs1060502466
ensemblrs1060502466
gopubmedrs1060502466
geneviewrs1060502466
scholarrs1060502466
googlers1060502466
pharmgkbrs1060502466
gwascentralrs1060502466
openSNPrs1060502466
23andMers1060502466
23andMe allrs1060502466
SNPshotrs1060502466
SNPdbers1060502466
MSV3drs1060502466
GWAS Ctlgrs1060502466
Max Magnitude0
ClinVar
Risk rs1060502466(C;C)
Alt rs1060502466(C;C)
Reference Rs1060502466(T;T)
Significance Probable-Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32910974T>C
CLNSRC
CLNACC RCV000463755.1, RCV000487989.1,