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rs876659212

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659212(-;-)
Make rs876659212(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61685908
GeneBRIP1
is asnp
is mentioned by
dbSNPrs876659212
ebirs876659212
HLIrs876659212
Exacrs876659212
Varsomers876659212
Maprs876659212
PheGenIrs876659212
hapmaprs876659212
1000 genomesrs876659212
hgdprs876659212
ensemblrs876659212
gopubmedrs876659212
geneviewrs876659212
scholarrs876659212
googlers876659212
pharmgkbrs876659212
gwascentralrs876659212
openSNPrs876659212
23andMers876659212
23andMe allrs876659212
SNP Nexus

SNPshotrs876659212
SNPdbers876659212
MSV3drs876659212
GWAS Ctlgrs876659212
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs876659212(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59763269delC
CLNSRC
CLNACC RCV000215452.1,