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rs775735278

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs775735278(-;-)
Make rs775735278(-;T)
Make rs775735278(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61784387
GeneBRIP1
is asnp
is mentioned by
dbSNPrs775735278
ebirs775735278
HLIrs775735278
Exacrs775735278
Varsomers775735278
Maprs775735278
PheGenIrs775735278
hapmaprs775735278
1000 genomesrs775735278
hgdprs775735278
ensemblrs775735278
gopubmedrs775735278
geneviewrs775735278
scholarrs775735278
googlers775735278
pharmgkbrs775735278
gwascentralrs775735278
openSNPrs775735278
23andMers775735278
23andMe allrs775735278
SNP Nexus

SNPshotrs775735278
SNPdbers775735278
MSV3drs775735278
GWAS Ctlgrs775735278
Max Magnitude0
ClinVar
Risk rs775735278(T;T)
Alt rs775735278(T;T)
Reference rs775735278(;)
Significance 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.59861749dupT
CLNSRC
CLNACC RCV000221659.1,