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rs786203485

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786203485(C;T)
Make rs786203485(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132579363
GeneRAD50
is asnp
is mentioned by
dbSNPrs786203485
ebirs786203485
HLIrs786203485
Exacrs786203485
Varsomers786203485
Maprs786203485
PheGenIrs786203485
hapmaprs786203485
1000 genomesrs786203485
hgdprs786203485
ensemblrs786203485
gopubmedrs786203485
geneviewrs786203485
scholarrs786203485
googlers786203485
pharmgkbrs786203485
gwascentralrs786203485
openSNPrs786203485
23andMers786203485
23andMe allrs786203485
SNP Nexus

SNPshotrs786203485
SNPdbers786203485
MSV3drs786203485
GWAS Ctlgrs786203485
Max Magnitude0
ClinVar
Risk rs786203485(T;T)
Alt rs786203485(T;T)
Reference rs786203485(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131915055C>T
CLNSRC
CLNACC RCV000166807.1,