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rs80359092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359092(A;A)
Make rs80359092(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370508
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359092
dbSNP (classic)rs80359092
ClinGenrs80359092
ebirs80359092
HLIrs80359092
Exacrs80359092
Gnomadrs80359092
Varsomers80359092
LitVarrs80359092
Maprs80359092
PheGenIrs80359092
Biobankrs80359092
1000 genomesrs80359092
hgdprs80359092
ensemblrs80359092
geneviewrs80359092
scholarrs80359092
googlers80359092
pharmgkbrs80359092
gwascentralrs80359092
openSNPrs80359092
23andMers80359092
SNPshotrs80359092
SNPdbers80359092
MSV3drs80359092
GWAS Ctlgrs80359092
Max Magnitude0
ClinVar
Risk rs80359092(A;A)
Alt rs80359092(A;A)
Reference Rs80359092(G;G)
Significance Untested
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32944645G>A
CLNSRC ClinVar
CLNACC RCV000045520.3, RCV000113933.1,