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rs80359185

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80359185(A;A)
Make rs80359185(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32380104
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359185
dbSNP (classic)rs80359185
ClinGenrs80359185
ebirs80359185
HLIrs80359185
Exacrs80359185
Gnomadrs80359185
Varsomers80359185
LitVarrs80359185
Maprs80359185
PheGenIrs80359185
Biobankrs80359185
1000 genomesrs80359185
hgdprs80359185
ensemblrs80359185
geneviewrs80359185
scholarrs80359185
googlers80359185
pharmgkbrs80359185
gwascentralrs80359185
openSNPrs80359185
23andMers80359185
SNPshotrs80359185
SNPdbers80359185
MSV3drs80359185
GWAS Ctlgrs80359185
Max Magnitude0
ClinVar
Risk rs80359185(A;A)
Alt rs80359185(A;A)
Reference Rs80359185(T;T)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer not specified
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 not specified
Reversed 0
HGVS NC_000013.10:g.32954241T>A
CLNSRC ClinVar
CLNACC RCV000045749.2, RCV000114067.1, RCV000481070.1,