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rs80356959

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80356959(C;C)
Make rs80356959(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045761
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80356959
ebirs80356959
HLIrs80356959
Exacrs80356959
Varsomers80356959
Maprs80356959
PheGenIrs80356959
hapmaprs80356959
1000 genomesrs80356959
hgdprs80356959
ensemblrs80356959
gopubmedrs80356959
geneviewrs80356959
scholarrs80356959
googlers80356959
pharmgkbrs80356959
gwascentralrs80356959
openSNPrs80356959
23andMers80356959
23andMe allrs80356959
SNP Nexus

SNPshotrs80356959
SNPdbers80356959
MSV3drs80356959
GWAS Ctlgrs80356959
Max Magnitude0
ClinVar
Risk rs80356959(C,G;C,G)
Alt rs80356959(C,G;C,G)
Reference rs80356959(T;T)
Significance Other
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000017.10:g.41197778A>C; NC_000017.10:g.41197778A>G
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000049027.2, RCV000112688.1, RCV000130013.2, RCV000031260.5, RCV000049026.2, RCV000129546.2, RCV000236322.1,