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rs876661246

From SNPedia

Orientationminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs876661246(-;-)
Make rs876661246(-;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61861538
GeneBRIP1
is asnp
is mentioned by
dbSNPrs876661246
ebirs876661246
HLIrs876661246
Exacrs876661246
Varsomers876661246
Maprs876661246
PheGenIrs876661246
hapmaprs876661246
1000 genomesrs876661246
hgdprs876661246
ensemblrs876661246
gopubmedrs876661246
geneviewrs876661246
scholarrs876661246
googlers876661246
pharmgkbrs876661246
gwascentralrs876661246
openSNPrs876661246
23andMers876661246
23andMe allrs876661246
SNP Nexus

SNPshotrs876661246
SNPdbers876661246
MSV3drs876661246
GWAS Ctlgrs876661246
Max Magnitude0
ClinVar
Risk rs876661246(;)
Alt rs876661246(;)
Reference rs876661246(AT;AT)
Significance Probable-Pathogenic
Disease not provided Familial cancer of breast Fanconi anemia
Variation info
Gene BRIP1
CLNDBN not provided Familial cancer of breast Fanconi anemia, complementation group J
Reversed 1
HGVS NC_000017.10:g.59938899_59938900delAT
CLNSRC
CLNACC RCV000221782.1, RCV000230644.1,