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rs80356863

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80356863(A;C)
Make rs80356863(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43115726
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80356863
ebirs80356863
HLIrs80356863
Exacrs80356863
Varsomers80356863
Maprs80356863
PheGenIrs80356863
hapmaprs80356863
1000 genomesrs80356863
hgdprs80356863
ensemblrs80356863
gopubmedrs80356863
geneviewrs80356863
scholarrs80356863
googlers80356863
pharmgkbrs80356863
gwascentralrs80356863
openSNPrs80356863
23andMers80356863
23andMe allrs80356863
SNP Nexus

SNPshotrs80356863
SNPdbers80356863
MSV3drs80356863
GWAS Ctlgrs80356863
Max Magnitude0
ClinVar
Risk rs80356863(C;C)
Alt rs80356863(C;C)
Reference rs80356863(A;A)
Significance Untested
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not specified
Reversed 1
HGVS NC_000017.10:g.41267743T>G
CLNSRC ClinVar
CLNACC RCV000030983.4, RCV000047432.5, RCV000166686.1, RCV000212155.1,