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rs878855145

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878855145(G;G)
Make rs878855145(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61744551
GeneBRIP1
is asnp
is mentioned by
dbSNPrs878855145
ebirs878855145
HLIrs878855145
Exacrs878855145
Varsomers878855145
Maprs878855145
PheGenIrs878855145
hapmaprs878855145
1000 genomesrs878855145
hgdprs878855145
ensemblrs878855145
gopubmedrs878855145
geneviewrs878855145
scholarrs878855145
googlers878855145
pharmgkbrs878855145
gwascentralrs878855145
openSNPrs878855145
23andMers878855145
23andMe allrs878855145
SNP Nexus

SNPshotrs878855145
SNPdbers878855145
MSV3drs878855145
GWAS Ctlgrs878855145
Max Magnitude0
ClinVar
Risk rs878855145(G;G)
Alt rs878855145(G;G)
Reference rs878855145(T;T)
Significance 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.59821912A>C
CLNSRC
CLNACC RCV000229169.1,