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rs80359100

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80359100(A;T)
Make rs80359100(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370556
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359100
dbSNP (classic)rs80359100
ClinGenrs80359100
ebirs80359100
HLIrs80359100
Exacrs80359100
Gnomadrs80359100
Varsomers80359100
LitVarrs80359100
Maprs80359100
PheGenIrs80359100
Biobankrs80359100
1000 genomesrs80359100
hgdprs80359100
ensemblrs80359100
geneviewrs80359100
scholarrs80359100
googlers80359100
pharmgkbrs80359100
gwascentralrs80359100
openSNPrs80359100
23andMers80359100
SNPshotrs80359100
SNPdbers80359100
MSV3drs80359100
GWAS Ctlgrs80359100
Max Magnitude0
ClinVar
Risk rs80359100(G;G) rs80359100(T;T)
Alt rs80359100(G;G) rs80359100(T;T)
Reference Rs80359100(A;A)
Significance Other
Disease Breast-ovarian cancer Familial cancer of breast Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32944693A>G; NC_000013.10:g.32944693A>T
CLNSRC ClinVar
CLNACC RCV000031744.6, RCV000045532.2, RCV000168607.2, RCV000045533.2, RCV000113943.1,