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rs748086984

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs748086984(A;A)
Make rs748086984(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132557455
GeneIL5, RAD50
is asnp
is mentioned by
dbSNPrs748086984
ebirs748086984
HLIrs748086984
Exacrs748086984
Varsomers748086984
Maprs748086984
PheGenIrs748086984
hapmaprs748086984
1000 genomesrs748086984
hgdprs748086984
ensemblrs748086984
gopubmedrs748086984
geneviewrs748086984
scholarrs748086984
googlers748086984
pharmgkbrs748086984
gwascentralrs748086984
openSNPrs748086984
23andMers748086984
23andMe allrs748086984
SNP Nexus

SNPshotrs748086984
SNPdbers748086984
MSV3drs748086984
GWAS Ctlgrs748086984
Max Magnitude0
ClinVar
Risk rs748086984(A;A)
Alt rs748086984(A;A)
Reference rs748086984(T;T)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene RAD50 IL5
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.131893147T>A
CLNSRC
CLNACC RCV000216511.1,