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

rs1060501968

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060501968(-;-)
Make rs1060501968(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position132595768
GeneRAD50
is asnp
is mentioned by
dbSNPrs1060501968
dbSNP (old)rs1060501968
ClinGenrs1060501968
ebirs1060501968
HLIrs1060501968
Exacrs1060501968
Gnomadrs1060501968
Varsomers1060501968
Maprs1060501968
PheGenIrs1060501968
Biobankrs1060501968
1000 genomesrs1060501968
hgdprs1060501968
ensemblrs1060501968
gopubmedrs1060501968
geneviewrs1060501968
scholarrs1060501968
googlers1060501968
pharmgkbrs1060501968
gwascentralrs1060501968
openSNPrs1060501968
23andMers1060501968
23andMe allrs1060501968
SNPshotrs1060501968
SNPdbers1060501968
MSV3drs1060501968
GWAS Ctlgrs1060501968
Max Magnitude0
ClinVar
Risk rs1060501968(-;-)
Alt rs1060501968(-;-)
Reference Rs1060501968(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131931460delA
CLNSRC
CLNACC RCV000471690.1,