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rs778664039

From SNPedia

Orientationplus
Geno Mag Summary
(ATAG;ATAG) 0 common in clinvar
Make rs778664039(-;-)
Make rs778664039(-;ATAG)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61683653
GeneBRIP1
is asnp
is mentioned by
dbSNPrs778664039
ebirs778664039
HLIrs778664039
Exacrs778664039
Varsomers778664039
Maprs778664039
PheGenIrs778664039
hapmaprs778664039
1000 genomesrs778664039
hgdprs778664039
ensemblrs778664039
gopubmedrs778664039
geneviewrs778664039
scholarrs778664039
googlers778664039
pharmgkbrs778664039
gwascentralrs778664039
openSNPrs778664039
23andMers778664039
23andMe allrs778664039
SNP Nexus

SNPshotrs778664039
SNPdbers778664039
MSV3drs778664039
GWAS Ctlgrs778664039
Max Magnitude0
ClinVar
Risk rs778664039(;)
Alt rs778664039(;)
Reference rs778664039(ATAG;ATAG)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRIP1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000017.10:g.59761014_59761017delATAG
CLNSRC
CLNACC RCV000219431.1,