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rs878854795

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878854795(-;-)
Make rs878854795(-;A)
Make rs878854795(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132609388
GeneRAD50
is asnp
is mentioned by
dbSNPrs878854795
ebirs878854795
HLIrs878854795
Exacrs878854795
Varsomers878854795
Maprs878854795
PheGenIrs878854795
hapmaprs878854795
1000 genomesrs878854795
hgdprs878854795
ensemblrs878854795
gopubmedrs878854795
geneviewrs878854795
scholarrs878854795
googlers878854795
pharmgkbrs878854795
gwascentralrs878854795
openSNPrs878854795
23andMers878854795
23andMe allrs878854795
SNP Nexus

SNPshotrs878854795
SNPdbers878854795
MSV3drs878854795
GWAS Ctlgrs878854795
Max Magnitude0
ClinVar
Risk rs878854795(A;A)
Alt rs878854795(A;A)
Reference rs878854795(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131945080dupA
CLNSRC
CLNACC RCV000231380.1,