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rs1060501949

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAGA;AAAGA) 0 common in clinvar
Make rs1060501949(-;-)
Make rs1060501949(-;AAAGA)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position132609345
GeneRAD50
is asnp
is mentioned by
dbSNPrs1060501949
dbSNP (old)rs1060501949
ClinGenrs1060501949
ebirs1060501949
HLIrs1060501949
Exacrs1060501949
Gnomadrs1060501949
Varsomers1060501949
Maprs1060501949
PheGenIrs1060501949
Biobankrs1060501949
1000 genomesrs1060501949
hgdprs1060501949
ensemblrs1060501949
gopubmedrs1060501949
geneviewrs1060501949
scholarrs1060501949
googlers1060501949
pharmgkbrs1060501949
gwascentralrs1060501949
openSNPrs1060501949
23andMers1060501949
23andMe allrs1060501949
SNPshotrs1060501949
SNPdbers1060501949
MSV3drs1060501949
GWAS Ctlgrs1060501949
Max Magnitude0
ClinVar
Risk rs1060501949(-;-)
Alt rs1060501949(-;-)
Reference Rs1060501949(AAAGA;AAAGA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131945037_131945041delAAAGA
CLNSRC
CLNACC RCV000463503.1,