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rs786203451

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203451(C;C)
Make rs786203451(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61693513
GeneBRIP1
is asnp
is mentioned by
dbSNPrs786203451
ebirs786203451
HLIrs786203451
Exacrs786203451
Varsomers786203451
Maprs786203451
PheGenIrs786203451
hapmaprs786203451
1000 genomesrs786203451
hgdprs786203451
ensemblrs786203451
gopubmedrs786203451
geneviewrs786203451
scholarrs786203451
googlers786203451
pharmgkbrs786203451
gwascentralrs786203451
openSNPrs786203451
23andMers786203451
23andMe allrs786203451
SNP Nexus

SNPshotrs786203451
SNPdbers786203451
MSV3drs786203451
GWAS Ctlgrs786203451
Max Magnitude0
ClinVar
Risk rs786203451(C;C)
Alt rs786203451(C;C)
Reference rs786203451(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.59770874C>G
CLNSRC
CLNACC RCV000166762.1,