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

rs80359064

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80359064(A;G)
Make rs80359064(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363379
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359064
ebirs80359064
HLIrs80359064
Exacrs80359064
Varsomers80359064
Maprs80359064
PheGenIrs80359064
hapmaprs80359064
1000 genomesrs80359064
hgdprs80359064
ensemblrs80359064
gopubmedrs80359064
geneviewrs80359064
scholarrs80359064
googlers80359064
pharmgkbrs80359064
gwascentralrs80359064
openSNPrs80359064
23andMers80359064
23andMe allrs80359064
SNP Nexus

SNPshotrs80359064
SNPdbers80359064
MSV3drs80359064
GWAS Ctlgrs80359064
Max Magnitude0
ClinVar
Risk rs80359064(G;G)
Alt rs80359064(G;G)
Reference rs80359064(A;A)
Significance Untested
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000013.10:g.32937516A>G
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000045442.5, RCV000077430.4, RCV000130671.2, RCV000212271.1,