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rs730881610

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;GA) 6 BRCA2 variant considered pathogenic for breast cancer
(GA;GA) 0 common in clinvar


Make rs730881610(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32339179
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730881610
ClinGenrs730881610
ebirs730881610
HLIrs730881610
Exacrs730881610
Varsomers730881610
Maprs730881610
PheGenIrs730881610
hapmaprs730881610
1000 genomesrs730881610
hgdprs730881610
ensemblrs730881610
gopubmedrs730881610
geneviewrs730881610
scholarrs730881610
googlers730881610
pharmgkbrs730881610
gwascentralrs730881610
openSNPrs730881610
23andMers730881610
23andMe allrs730881610
SNP Nexus

SNPshotrs730881610
SNPdbers730881610
MSV3drs730881610
GWAS Ctlgrs730881610
Max Magnitude6
ClinVar
Risk rs730881610(-;-)
Alt rs730881610(-;-)
Reference Rs730881610(GA;GA)
Significance Pathogenic
Disease not provided Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN not provided Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913316_32913317delGA
CLNSRC
CLNACC RCV000160292.2, RCV000241101.1,