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rs878855150

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878855150(-;-)
Make rs878855150(-;CAAA)
Make rs878855150(CAAA;CAAA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61684052
GeneBRIP1
is asnp
is mentioned by
dbSNPrs878855150
ebirs878855150
HLIrs878855150
Exacrs878855150
Varsomers878855150
Maprs878855150
PheGenIrs878855150
hapmaprs878855150
1000 genomesrs878855150
hgdprs878855150
ensemblrs878855150
gopubmedrs878855150
geneviewrs878855150
scholarrs878855150
googlers878855150
pharmgkbrs878855150
gwascentralrs878855150
openSNPrs878855150
23andMers878855150
23andMe allrs878855150
SNP Nexus

SNPshotrs878855150
SNPdbers878855150
MSV3drs878855150
GWAS Ctlgrs878855150
Max Magnitude0
ClinVar
Risk rs878855150(CAAA;CAAA)
Alt rs878855150(CAAA;CAAA)
Reference rs878855150(;)
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_59761417dupTTTG
CLNSRC
CLNACC RCV000233395.1,