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

rs786203151

From SNPedia

Orientationplus
Geno Mag Summary
(AGAC;AGAC) 0 common in clinvar
Make rs786203151(-;-)
Make rs786203151(-;ACAG)
Make rs786203151(ACAG;ACAG)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132591315
GeneRAD50
is asnp
is mentioned by
dbSNPrs786203151
ebirs786203151
HLIrs786203151
Exacrs786203151
Varsomers786203151
Maprs786203151
PheGenIrs786203151
hapmaprs786203151
1000 genomesrs786203151
hgdprs786203151
ensemblrs786203151
gopubmedrs786203151
geneviewrs786203151
scholarrs786203151
googlers786203151
pharmgkbrs786203151
gwascentralrs786203151
openSNPrs786203151
23andMers786203151
23andMe allrs786203151
SNP Nexus

SNPshotrs786203151
SNPdbers786203151
MSV3drs786203151
GWAS Ctlgrs786203151
Max Magnitude0
ClinVar
Risk rs786203151(;)
Alt rs786203151(;)
Reference rs786203151(AGAC;AGAC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131927007_131927010delACAG
CLNSRC
CLNACC RCV000166330.1,