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rs878855151

From SNPedia

Orientationminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs878855151(-;-)
Make rs878855151(-;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61684053
GeneBRIP1
is asnp
is mentioned by
dbSNPrs878855151
ebirs878855151
HLIrs878855151
Exacrs878855151
Varsomers878855151
Maprs878855151
PheGenIrs878855151
hapmaprs878855151
1000 genomesrs878855151
hgdprs878855151
ensemblrs878855151
gopubmedrs878855151
geneviewrs878855151
scholarrs878855151
googlers878855151
pharmgkbrs878855151
gwascentralrs878855151
openSNPrs878855151
23andMers878855151
23andMe allrs878855151
SNP Nexus

SNPshotrs878855151
SNPdbers878855151
MSV3drs878855151
GWAS Ctlgrs878855151
Max Magnitude0
ClinVar
Risk rs878855151(;)
Alt rs878855151(;)
Reference rs878855151(AA;AA)
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.59761414_59761415delTT
CLNSRC
CLNACC RCV000227245.1,