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rs80359027

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359027(A;A)
Make rs80359027(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362693
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359027
ebirs80359027
HLIrs80359027
Exacrs80359027
Varsomers80359027
Maprs80359027
PheGenIrs80359027
hapmaprs80359027
1000 genomesrs80359027
hgdprs80359027
ensemblrs80359027
gopubmedrs80359027
geneviewrs80359027
scholarrs80359027
googlers80359027
pharmgkbrs80359027
gwascentralrs80359027
openSNPrs80359027
23andMers80359027
23andMe allrs80359027
SNP Nexus

SNPshotrs80359027
SNPdbers80359027
MSV3drs80359027
GWAS Ctlgrs80359027
Max Magnitude0
ClinVar
Risk rs80359027(A,C;A,C)
Alt rs80359027(A,C;A,C)
Reference rs80359027(G;G)
Significance Other
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32936830G>A; NC_000013.10:g.32936830G>C
CLNSRC Inc.
CLNACC RCV000031713.6, RCV000045366.5, RCV000131687.3, RCV000212266.1, RCV000045367.2, RCV000113849.2,