Have questions? Visit https://www.reddit.com/r/SNPedia

rs80359635

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs80359635(-;-)
Make rs80359635(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32354885
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359635
ebirs80359635
HLIrs80359635
Exacrs80359635
Varsomers80359635
Maprs80359635
PheGenIrs80359635
hapmaprs80359635
1000 genomesrs80359635
hgdprs80359635
ensemblrs80359635
gopubmedrs80359635
geneviewrs80359635
scholarrs80359635
googlers80359635
pharmgkbrs80359635
gwascentralrs80359635
openSNPrs80359635
23andMers80359635
23andMe allrs80359635
SNP Nexus

SNPshotrs80359635
SNPdbers80359635
MSV3drs80359635
GWAS Ctlgrs80359635
Max Magnitude6
rs80359635, also known as 7260insA, c.7032_7033insA and p.Ile2344_Gln2345?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359635(A;A)
Alt rs80359635(A;A)
Reference rs80359635(;)
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.32929022dupA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045125.2, RCV000113694.1,