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rs80359029

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80359029(G;G)
Make rs80359029(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363180
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359029
ebirs80359029
HLIrs80359029
Exacrs80359029
Varsomers80359029
Maprs80359029
PheGenIrs80359029
hapmaprs80359029
1000 genomesrs80359029
hgdprs80359029
ensemblrs80359029
gopubmedrs80359029
geneviewrs80359029
scholarrs80359029
googlers80359029
pharmgkbrs80359029
gwascentralrs80359029
openSNPrs80359029
23andMers80359029
23andMe allrs80359029
SNP Nexus

SNPshotrs80359029
SNPdbers80359029
MSV3drs80359029
GWAS Ctlgrs80359029
Max Magnitude0
ClinVar
Risk rs80359029(G;G)
Alt rs80359029(G;G)
Reference rs80359029(T;T)
Significance Other
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.32937317T>G
CLNSRC ClinVar
CLNACC RCV000045371.2, RCV000077420.4,