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rs786201733

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786201733(C;T)
Make rs786201733(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61808718
GeneBRIP1
is asnp
is mentioned by
dbSNPrs786201733
ebirs786201733
HLIrs786201733
Exacrs786201733
Varsomers786201733
Maprs786201733
PheGenIrs786201733
hapmaprs786201733
1000 genomesrs786201733
hgdprs786201733
ensemblrs786201733
gopubmedrs786201733
geneviewrs786201733
scholarrs786201733
googlers786201733
pharmgkbrs786201733
gwascentralrs786201733
openSNPrs786201733
23andMers786201733
23andMe allrs786201733
SNP Nexus

SNPshotrs786201733
SNPdbers786201733
MSV3drs786201733
GWAS Ctlgrs786201733
Max Magnitude0
ClinVar
Risk rs786201733(T;T)
Alt rs786201733(T;T)
Reference rs786201733(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59886079G>A
CLNSRC
CLNACC RCV000164174.1,