Have questions? Visit https://www.reddit.com/r/SNPedia

rs878855134

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878855134(-;-)
Make rs878855134(-;CT)
Make rs878855134(CT;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61801374
GeneBRIP1
is asnp
is mentioned by
dbSNPrs878855134
ebirs878855134
HLIrs878855134
Exacrs878855134
Varsomers878855134
Maprs878855134
PheGenIrs878855134
hapmaprs878855134
1000 genomesrs878855134
hgdprs878855134
ensemblrs878855134
gopubmedrs878855134
geneviewrs878855134
scholarrs878855134
googlers878855134
pharmgkbrs878855134
gwascentralrs878855134
openSNPrs878855134
23andMers878855134
23andMe allrs878855134
SNP Nexus

SNPshotrs878855134
SNPdbers878855134
MSV3drs878855134
GWAS Ctlgrs878855134
Max Magnitude0
ClinVar
Risk rs878855134(CT;CT)
Alt rs878855134(CT;CT)
Reference rs878855134(;)
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.59878735_59878736insAG
CLNSRC
CLNACC RCV000234635.1,