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rs869312762

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312762(-;-)
Make rs869312762(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61784423
GeneBRIP1
is asnp
is mentioned by
dbSNPrs869312762
ebirs869312762
HLIrs869312762
Exacrs869312762
Varsomers869312762
Maprs869312762
PheGenIrs869312762
hapmaprs869312762
1000 genomesrs869312762
hgdprs869312762
ensemblrs869312762
gopubmedrs869312762
geneviewrs869312762
scholarrs869312762
googlers869312762
pharmgkbrs869312762
gwascentralrs869312762
openSNPrs869312762
23andMers869312762
23andMe allrs869312762
SNP Nexus

SNPshotrs869312762
SNPdbers869312762
MSV3drs869312762
GWAS Ctlgrs869312762
Max Magnitude0
ClinVar
Risk rs869312762(;)
Alt rs869312762(;)
Reference rs869312762(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59861784delC
CLNSRC
CLNACC RCV000210200.1,