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rs878855159

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878855159(-;-)
Make rs878855159(-;T)
Make rs878855159(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61808494
GeneBRIP1
is asnp
is mentioned by
dbSNPrs878855159
ebirs878855159
HLIrs878855159
Exacrs878855159
Varsomers878855159
Maprs878855159
PheGenIrs878855159
hapmaprs878855159
1000 genomesrs878855159
hgdprs878855159
ensemblrs878855159
gopubmedrs878855159
geneviewrs878855159
scholarrs878855159
googlers878855159
pharmgkbrs878855159
gwascentralrs878855159
openSNPrs878855159
23andMers878855159
23andMe allrs878855159
SNP Nexus

SNPshotrs878855159
SNPdbers878855159
MSV3drs878855159
GWAS Ctlgrs878855159
Max Magnitude0
ClinVar
Risk rs878855159(T;T)
Alt rs878855159(T;T)
Reference rs878855159(;)
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.59885855_59885856insA
CLNSRC
CLNACC RCV000232385.1,