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rs786203521

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786203521(-;-)
Make rs786203521(-;A)
Make rs786203521(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61849195
GeneBRIP1
is asnp
is mentioned by
dbSNPrs786203521
ebirs786203521
HLIrs786203521
Exacrs786203521
Varsomers786203521
Maprs786203521
PheGenIrs786203521
hapmaprs786203521
1000 genomesrs786203521
hgdprs786203521
ensemblrs786203521
gopubmedrs786203521
geneviewrs786203521
scholarrs786203521
googlers786203521
pharmgkbrs786203521
gwascentralrs786203521
openSNPrs786203521
23andMers786203521
23andMe allrs786203521
SNP Nexus

SNPshotrs786203521
SNPdbers786203521
MSV3drs786203521
GWAS Ctlgrs786203521
Max Magnitude0
ClinVar
Risk rs786203521(A;A)
Alt rs786203521(A;A)
Reference rs786203521(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59926557dupT
CLNSRC
CLNACC RCV000166862.1,