Have questions? Visit https://www.reddit.com/r/SNPedia

rs28903098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0
Make rs28903098(C;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position61859862
GeneBRIP1
is asnp
is mentioned by
dbSNPrs28903098
ebirs28903098
HLIrs28903098
Exacrs28903098
Varsomers28903098
Maprs28903098
PheGenIrs28903098
hapmaprs28903098
1000 genomesrs28903098
hgdprs28903098
ensemblrs28903098
gopubmedrs28903098
geneviewrs28903098
scholarrs28903098
googlers28903098
pharmgkbrs28903098
gwascentralrs28903098
openSNPrs28903098
23andMers28903098
23andMe allrs28903098
SNP Nexus

SNPshotrs28903098
SNPdbers28903098
MSV3drs28903098
GWAS Ctlgrs28903098
Merged fromRs137852984
Max Magnitude0
OMIM605882
DescBREAST CANCER, EARLY-ONSET
Variant0001
Relatedalso


ClinVar
Risk rs28903098(A,G;A,G)
Alt rs28903098(A,G;A,G)
Reference rs28903098(C;C)
Significance Pathogenic
Disease Breast cancer Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRIP1
CLNDBN Breast cancer, early-onset Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia, complementation group J not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.59937223G>C; NC_000017.10:g.59937223G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005002.2, RCV000116124.6, RCV000199377.3, RCV000200979.2, RCV000160330.2, RCV000216538.1,