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

rs587780150

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780150(C;T)
Make rs587780150(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132589778
GeneRAD50
is asnp
is mentioned by
dbSNPrs587780150
ebirs587780150
HLIrs587780150
Exacrs587780150
Varsomers587780150
Maprs587780150
PheGenIrs587780150
hapmaprs587780150
1000 genomesrs587780150
hgdprs587780150
ensemblrs587780150
gopubmedrs587780150
geneviewrs587780150
scholarrs587780150
googlers587780150
pharmgkbrs587780150
gwascentralrs587780150
openSNPrs587780150
23andMers587780150
23andMe allrs587780150
SNP Nexus

SNPshotrs587780150
SNPdbers587780150
MSV3drs587780150
GWAS Ctlgrs587780150
Max Magnitude0
ClinVar
Risk rs587780150(T;T)
Alt rs587780150(T;T)
Reference rs587780150(C;C)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene RAD50
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.131925470C>T
CLNSRC
CLNACC RCV000115933.3, RCV000222369.1,