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rs730882169

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730882169(A;A)
Make rs730882169(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32355119
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730882169
ebirs730882169
HLIrs730882169
Exacrs730882169
Varsomers730882169
Maprs730882169
PheGenIrs730882169
hapmaprs730882169
1000 genomesrs730882169
hgdprs730882169
ensemblrs730882169
gopubmedrs730882169
geneviewrs730882169
scholarrs730882169
googlers730882169
pharmgkbrs730882169
gwascentralrs730882169
openSNPrs730882169
23andMers730882169
23andMe allrs730882169
SNP Nexus

SNPshotrs730882169
SNPdbers730882169
MSV3drs730882169
GWAS Ctlgrs730882169
Max Magnitude0
ClinVar
Risk rs730882169(A;A)
Alt rs730882169(A;A)
Reference rs730882169(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32929256T>A
CLNSRC
CLNACC RCV000162058.1,