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rs587780226

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780226(C;T)
Make rs587780226(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61799125
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587780226
ebirs587780226
HLIrs587780226
Exacrs587780226
Varsomers587780226
Maprs587780226
PheGenIrs587780226
hapmaprs587780226
1000 genomesrs587780226
hgdprs587780226
ensemblrs587780226
gopubmedrs587780226
geneviewrs587780226
scholarrs587780226
googlers587780226
pharmgkbrs587780226
gwascentralrs587780226
openSNPrs587780226
23andMers587780226
23andMe allrs587780226
SNP Nexus

SNPshotrs587780226
SNPdbers587780226
MSV3drs587780226
GWAS Ctlgrs587780226
Max Magnitude0
ClinVar
Risk rs587780226(T;T)
Alt rs587780226(T;T)
Reference rs587780226(C;C)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRIP1
CLNDBN not provided Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.59876486G>A
CLNSRC
CLNACC RCV000116121.4, RCV000210150.1, RCV000216285.1,