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rs55851803

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs55851803(A;A)
Make rs55851803(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43106477
GeneBRCA1
is asnp
is mentioned by
dbSNPrs55851803
ebirs55851803
HLIrs55851803
Exacrs55851803
Varsomers55851803
Maprs55851803
PheGenIrs55851803
hapmaprs55851803
1000 genomesrs55851803
hgdprs55851803
ensemblrs55851803
gopubmedrs55851803
geneviewrs55851803
scholarrs55851803
googlers55851803
pharmgkbrs55851803
gwascentralrs55851803
openSNPrs55851803
23andMers55851803
23andMe allrs55851803
SNP Nexus

SNPshotrs55851803
SNPdbers55851803
MSV3drs55851803
GWAS Ctlgrs55851803
Max Magnitude0
ClinVar
Risk rs55851803(A;A)
Alt rs55851803(A;A)
Reference rs55851803(G;G)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000017.10:g.41258494C>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000047641.3, RCV000077501.5, RCV000131896.2, RCV000236464.1,