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rs730881607

From SNPedia

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


Make rs730881607(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32338523
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730881607
dbSNP (old)rs730881607
ClinGenrs730881607
ebirs730881607
HLIrs730881607
Exacrs730881607
Varsomers730881607
Maprs730881607
PheGenIrs730881607
Biobankrs730881607
1000 genomesrs730881607
hgdprs730881607
ensemblrs730881607
gopubmedrs730881607
geneviewrs730881607
scholarrs730881607
googlers730881607
pharmgkbrs730881607
gwascentralrs730881607
openSNPrs730881607
23andMers730881607
23andMe allrs730881607
SNP Nexus

SNPshotrs730881607
SNPdbers730881607
MSV3drs730881607
GWAS Ctlgrs730881607
Max Magnitude6
ClinVar
Risk rs730881607(-;-)
Alt rs730881607(-;-)
Reference Rs730881607(TT;TT)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912660_32912661delTT
CLNSRC
CLNACC RCV000160285.1, RCV000241006.2,