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rs786201531

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786201531(-;-)
Make rs786201531(-;T)
Make rs786201531(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132579492
GeneRAD50
is asnp
is mentioned by
dbSNPrs786201531
ebirs786201531
HLIrs786201531
Exacrs786201531
Varsomers786201531
Maprs786201531
PheGenIrs786201531
hapmaprs786201531
1000 genomesrs786201531
hgdprs786201531
ensemblrs786201531
gopubmedrs786201531
geneviewrs786201531
scholarrs786201531
googlers786201531
pharmgkbrs786201531
gwascentralrs786201531
openSNPrs786201531
23andMers786201531
23andMe allrs786201531
SNP Nexus

SNPshotrs786201531
SNPdbers786201531
MSV3drs786201531
GWAS Ctlgrs786201531
Max Magnitude0
ClinVar
Risk rs786201531(T;T)
Alt rs786201531(T;T)
Reference rs786201531(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131915184dupT
CLNSRC
CLNACC RCV000163823.3,