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rs869312763

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312763(A;G)
Make rs869312763(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61686167
GeneBRIP1
is asnp
is mentioned by
dbSNPrs869312763
ebirs869312763
HLIrs869312763
Exacrs869312763
Varsomers869312763
Maprs869312763
PheGenIrs869312763
hapmaprs869312763
1000 genomesrs869312763
hgdprs869312763
ensemblrs869312763
gopubmedrs869312763
geneviewrs869312763
scholarrs869312763
googlers869312763
pharmgkbrs869312763
gwascentralrs869312763
openSNPrs869312763
23andMers869312763
23andMe allrs869312763
SNP Nexus

SNPshotrs869312763
SNPdbers869312763
MSV3drs869312763
GWAS Ctlgrs869312763
Max Magnitude0
ClinVar
Risk rs869312763(G;G)
Alt rs869312763(G;G)
Reference rs869312763(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59763528T>C
CLNSRC
CLNACC RCV000210117.1,