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rs878855143

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878855143(A;G)
Make rs878855143(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61776564
GeneBRIP1
is asnp
is mentioned by
dbSNPrs878855143
ebirs878855143
HLIrs878855143
Exacrs878855143
Varsomers878855143
Maprs878855143
PheGenIrs878855143
hapmaprs878855143
1000 genomesrs878855143
hgdprs878855143
ensemblrs878855143
gopubmedrs878855143
geneviewrs878855143
scholarrs878855143
googlers878855143
pharmgkbrs878855143
gwascentralrs878855143
openSNPrs878855143
23andMers878855143
23andMe allrs878855143
SNP Nexus

SNPshotrs878855143
SNPdbers878855143
MSV3drs878855143
GWAS Ctlgrs878855143
Max Magnitude0
ClinVar
Risk rs878855143(G;G)
Alt rs878855143(G;G)
Reference rs878855143(A;A)
Significance Probable-Pathogenic
Disease Familial cancer of breast Fanconi anemia
Variation info
Gene BRIP1
CLNDBN Familial cancer of breast Fanconi anemia, complementation group J
Reversed 1
HGVS NC_000017.10:g.59853925T>C
CLNSRC
CLNACC RCV000232507.1,