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rs869312759

From SNPedia

Orientationplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs869312759(-;-)
Make rs869312759(-;CT)
Make rs869312759(CT;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338044
GeneBRCA2
is asnp
is mentioned by
dbSNPrs869312759
ebirs869312759
HLIrs869312759
Exacrs869312759
Varsomers869312759
Maprs869312759
PheGenIrs869312759
hapmaprs869312759
1000 genomesrs869312759
hgdprs869312759
ensemblrs869312759
gopubmedrs869312759
geneviewrs869312759
scholarrs869312759
googlers869312759
pharmgkbrs869312759
gwascentralrs869312759
openSNPrs869312759
23andMers869312759
23andMe allrs869312759
SNP Nexus

SNPshotrs869312759
SNPdbers869312759
MSV3drs869312759
GWAS Ctlgrs869312759
Max Magnitude0
ClinVar
Risk rs869312759(;)
Alt rs869312759(;)
Reference rs869312759(TC;TC)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 1
Reversed 0
HGVS NC_000013.10:g.32912181_32912182delCT
CLNSRC
CLNACC RCV000210084.1,