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rs878853297

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs878853297(-;-)
Make rs878853297(-;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32319169
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853297
ebirs878853297
HLIrs878853297
Exacrs878853297
Varsomers878853297
Maprs878853297
PheGenIrs878853297
hapmaprs878853297
1000 genomesrs878853297
hgdprs878853297
ensemblrs878853297
gopubmedrs878853297
geneviewrs878853297
scholarrs878853297
googlers878853297
pharmgkbrs878853297
gwascentralrs878853297
openSNPrs878853297
23andMers878853297
23andMe allrs878853297
SNP Nexus

SNPshotrs878853297
SNPdbers878853297
MSV3drs878853297
GWAS Ctlgrs878853297
Max Magnitude0
ClinVar
Risk rs878853297(;)
Alt rs878853297(;)
Reference rs878853297(AA;AA)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32893306_32893307delAA
CLNSRC
CLNACC RCV000225394.1,