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rs80358985

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80358985(C;T)
Make rs80358985(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32356557
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80358985
ebirs80358985
HLIrs80358985
Exacrs80358985
Varsomers80358985
Maprs80358985
PheGenIrs80358985
hapmaprs80358985
1000 genomesrs80358985
hgdprs80358985
ensemblrs80358985
gopubmedrs80358985
geneviewrs80358985
scholarrs80358985
googlers80358985
pharmgkbrs80358985
gwascentralrs80358985
openSNPrs80358985
23andMers80358985
23andMe allrs80358985
SNP Nexus

SNPshotrs80358985
SNPdbers80358985
MSV3drs80358985
GWAS Ctlgrs80358985
Max Magnitude0
ClinVar
Risk rs80358985(T;T)
Alt rs80358985(T;T)
Reference rs80358985(C;C)
Significance Other
Disease Breast-ovarian cancer Familial cancer of breast Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000013.10:g.32930694C>T
CLNSRC ClinVar
CLNACC RCV000031686.6, RCV000045249.4, RCV000162600.1, RCV000212261.1,