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rs80359104

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80359104(C;T)
Make rs80359104(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370992
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359104
ebirs80359104
HLIrs80359104
Exacrs80359104
Varsomers80359104
Maprs80359104
PheGenIrs80359104
hapmaprs80359104
1000 genomesrs80359104
hgdprs80359104
ensemblrs80359104
gopubmedrs80359104
geneviewrs80359104
scholarrs80359104
googlers80359104
pharmgkbrs80359104
gwascentralrs80359104
openSNPrs80359104
23andMers80359104
23andMe allrs80359104
SNP Nexus

SNPshotrs80359104
SNPdbers80359104
MSV3drs80359104
GWAS Ctlgrs80359104
Max Magnitude0
ClinVar
Risk rs80359104(T;T)
Alt rs80359104(T;T)
Reference rs80359104(C;C)
Significance Other
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.32945129C>T
CLNSRC ClinVar
CLNACC RCV000045544.5, RCV000077443.5, RCV000165225.1, RCV000212277.1,