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rs869312760

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATCGCTTTTCA;ATCGCTTTTCA) 0 common in clinvar
(TCATCGCTTT;TCATCGCTTT) 0 common in clinvar
Make rs869312760(-;-)
Make rs869312760(-;TCGCTTTTCA)
Make rs869312760(TCGCTTTTCA;TCGCTTTTCA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32370489
GeneBRCA2
is asnp
is mentioned by
dbSNPrs869312760
dbSNP (old)rs869312760
ClinGenrs869312760
ebirs869312760
HLIrs869312760
Exacrs869312760
Gnomadrs869312760
Varsomers869312760
Maprs869312760
PheGenIrs869312760
Biobankrs869312760
1000 genomesrs869312760
hgdprs869312760
ensemblrs869312760
gopubmedrs869312760
geneviewrs869312760
scholarrs869312760
googlers869312760
pharmgkbrs869312760
gwascentralrs869312760
openSNPrs869312760
23andMers869312760
23andMe allrs869312760
SNP Nexus

SNPshotrs869312760
SNPdbers869312760
MSV3drs869312760
GWAS Ctlgrs869312760
Max Magnitude0
ClinVar
Risk rs869312760(-;-)
Alt rs869312760(-;-)
Reference Rs869312760(TCATCGCTTT;TCATCGCTTT)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 1
Reversed 0
HGVS NC_000013.10:g.32944626_32944635delTCGCTTTTCA
CLNSRC
CLNACC RCV000210188.1,