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rs80359153

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80359153(A;T)
Make rs80359153(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379802
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359153
ebirs80359153
HLIrs80359153
Exacrs80359153
Varsomers80359153
Maprs80359153
PheGenIrs80359153
hapmaprs80359153
1000 genomesrs80359153
hgdprs80359153
ensemblrs80359153
gopubmedrs80359153
geneviewrs80359153
scholarrs80359153
googlers80359153
pharmgkbrs80359153
gwascentralrs80359153
openSNPrs80359153
23andMers80359153
23andMe allrs80359153
SNP Nexus

SNPshotrs80359153
SNPdbers80359153
MSV3drs80359153
GWAS Ctlgrs80359153
Max Magnitude0
ClinVar
Risk rs80359153(T;T)
Alt rs80359153(T;T)
Reference rs80359153(A;A)
Significance Other
Disease Hereditary breast and ovarian cancer syndrome not specified Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome not specified Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32953939A>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000045686.2, RCV000074558.6, RCV000083151.4, RCV000129004.2,