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rs80359669

From SNPedia

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


Make rs80359669(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357779
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359669
ebirs80359669
HLIrs80359669
Exacrs80359669
Varsomers80359669
Maprs80359669
PheGenIrs80359669
hapmaprs80359669
1000 genomesrs80359669
hgdprs80359669
ensemblrs80359669
gopubmedrs80359669
geneviewrs80359669
scholarrs80359669
googlers80359669
pharmgkbrs80359669
gwascentralrs80359669
openSNPrs80359669
23andMers80359669
23andMe allrs80359669
SNP Nexus

SNPshotrs80359669
SNPdbers80359669
MSV3drs80359669
GWAS Ctlgrs80359669
Max Magnitude6
rs80359669, also known as 7883del4, c.7655_7658delTTAA and p.Ile2552_Asn2553?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359669(;)
Alt rs80359669(;)
Reference rs80359669(AATT;AATT)
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.32931916_32931919delTTAA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045277.2, RCV000113803.1,