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rs876660728

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660728(A;G)
Make rs876660728(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132595571
GeneRAD50
is asnp
is mentioned by
dbSNPrs876660728
ebirs876660728
HLIrs876660728
Exacrs876660728
Varsomers876660728
Maprs876660728
PheGenIrs876660728
hapmaprs876660728
1000 genomesrs876660728
hgdprs876660728
ensemblrs876660728
gopubmedrs876660728
geneviewrs876660728
scholarrs876660728
googlers876660728
pharmgkbrs876660728
gwascentralrs876660728
openSNPrs876660728
23andMers876660728
23andMe allrs876660728
SNP Nexus

SNPshotrs876660728
SNPdbers876660728
MSV3drs876660728
GWAS Ctlgrs876660728
Max Magnitude0
ClinVar
Risk rs876660728(G;G)
Alt rs876660728(G;G)
Reference rs876660728(A;A)
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.131931263A>G
CLNSRC
CLNACC RCV000216775.1,