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rs876659707

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 6 Ovarian cancer susceptibility
Make rs876659707(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61847222
GeneBRIP1
is asnp
is mentioned by
dbSNPrs876659707
dbSNP (classic)rs876659707
ClinGenrs876659707
ebirs876659707
HLIrs876659707
Exacrs876659707
Gnomadrs876659707
Varsomers876659707
LitVarrs876659707
Maprs876659707
PheGenIrs876659707
Biobankrs876659707
1000 genomesrs876659707
hgdprs876659707
ensemblrs876659707
geneviewrs876659707
scholarrs876659707
googlers876659707
pharmgkbrs876659707
gwascentralrs876659707
openSNPrs876659707
23andMers876659707
SNPshotrs876659707
SNPdbers876659707
MSV3drs876659707
GWAS Ctlgrs876659707
Max Magnitude6
ClinVar
Risk rs876659707(T;T)
Alt rs876659707(T;T)
Reference Rs876659707(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.59924583T>A
CLNSRC
CLNACC RCV000214929.1,