Have questions? Visit https://www.reddit.com/r/SNPedia

rs786203429

From SNPedia

Orientationminus
Geno Mag Summary
(ATA;ATA) 0 common in clinvar
Make rs786203429(ATA;CT)
Make rs786203429(CT;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61849196
GeneBRIP1
is asnp
is mentioned by
dbSNPrs786203429
ebirs786203429
HLIrs786203429
Exacrs786203429
Varsomers786203429
Maprs786203429
PheGenIrs786203429
hapmaprs786203429
1000 genomesrs786203429
hgdprs786203429
ensemblrs786203429
gopubmedrs786203429
geneviewrs786203429
scholarrs786203429
googlers786203429
pharmgkbrs786203429
gwascentralrs786203429
openSNPrs786203429
23andMers786203429
23andMe allrs786203429
SNP Nexus

SNPshotrs786203429
SNPdbers786203429
MSV3drs786203429
GWAS Ctlgrs786203429
Max Magnitude0
ClinVar
Risk rs786203429(CT;CT)
Alt rs786203429(CT;CT)
Reference rs786203429(ATA;ATA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59926557_59926559delTATinsAG
CLNSRC
CLNACC RCV000166730.1,