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rs786203717

From SNPedia

Orientationminus
Geno Mag Summary
(AAGA;AAGA) 0 common in clinvar
Make rs786203717(-;-)
Make rs786203717(-;AAGA)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61684051
GeneBRIP1
is asnp
is mentioned by
dbSNPrs786203717
ebirs786203717
HLIrs786203717
Exacrs786203717
Varsomers786203717
Maprs786203717
PheGenIrs786203717
hapmaprs786203717
1000 genomesrs786203717
hgdprs786203717
ensemblrs786203717
gopubmedrs786203717
geneviewrs786203717
scholarrs786203717
googlers786203717
pharmgkbrs786203717
gwascentralrs786203717
openSNPrs786203717
23andMers786203717
23andMe allrs786203717
SNP Nexus

SNPshotrs786203717
SNPdbers786203717
MSV3drs786203717
GWAS Ctlgrs786203717
Max Magnitude0
ClinVar
Risk rs786203717(;)
Alt rs786203717(;)
Reference rs786203717(AAGA;AAGA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59761412_59761415delTCTT
CLNSRC
CLNACC RCV000167141.1,