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rs80359666

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;TT) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs80359666(-;-)
Make rs80359666(TT;TT)
ReferenceGRCh38 38.1/142
Chromosome13
Position32356587
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359666
ebirs80359666
HLIrs80359666
Exacrs80359666
Varsomers80359666
Maprs80359666
PheGenIrs80359666
hapmaprs80359666
1000 genomesrs80359666
hgdprs80359666
ensemblrs80359666
gopubmedrs80359666
geneviewrs80359666
scholarrs80359666
googlers80359666
pharmgkbrs80359666
gwascentralrs80359666
openSNPrs80359666
23andMers80359666
23andMe allrs80359666
SNP Nexus

SNPshotrs80359666
SNPdbers80359666
MSV3drs80359666
GWAS Ctlgrs80359666
Max Magnitude6
rs80359666, also known as 7823insTT, c.7595_7596insTT and p.Pro2532?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359666(TT;TT)
Alt rs80359666(TT;TT)
Reference rs80359666(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32930724_32930725insTT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113779.1,