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rs876659158

From SNPedia

Orientationplus
Geno Mag Summary
(AAGGT;AAGGT) 0 common in clinvar
Make rs876659158(-;-)
Make rs876659158(-;GTAAG)
Make rs876659158(GTAAG;GTAAG)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132605000
GeneRAD50
is asnp
is mentioned by
dbSNPrs876659158
ebirs876659158
HLIrs876659158
Exacrs876659158
Varsomers876659158
Maprs876659158
PheGenIrs876659158
hapmaprs876659158
1000 genomesrs876659158
hgdprs876659158
ensemblrs876659158
gopubmedrs876659158
geneviewrs876659158
scholarrs876659158
googlers876659158
pharmgkbrs876659158
gwascentralrs876659158
openSNPrs876659158
23andMers876659158
23andMe allrs876659158
SNP Nexus

SNPshotrs876659158
SNPdbers876659158
MSV3drs876659158
GWAS Ctlgrs876659158
Max Magnitude0
ClinVar
Risk rs876659158(;)
Alt rs876659158(;)
Reference rs876659158(AAGGT;AAGGT)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene RAD50
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.131940692_131940696delGTAAG
CLNSRC
CLNACC RCV000220659.1,