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rs786203773

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786203773(-;-)
Make rs786203773(-;GA)
Make rs786203773(GA;GA)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132588844
GeneRAD50
is asnp
is mentioned by
dbSNPrs786203773
ebirs786203773
HLIrs786203773
Exacrs786203773
Varsomers786203773
Maprs786203773
PheGenIrs786203773
hapmaprs786203773
1000 genomesrs786203773
hgdprs786203773
ensemblrs786203773
gopubmedrs786203773
geneviewrs786203773
scholarrs786203773
googlers786203773
pharmgkbrs786203773
gwascentralrs786203773
openSNPrs786203773
23andMers786203773
23andMe allrs786203773
SNP Nexus

SNPshotrs786203773
SNPdbers786203773
MSV3drs786203773
GWAS Ctlgrs786203773
Max Magnitude0
ClinVar
Risk rs786203773(GA;GA)
Alt rs786203773(GA;GA)
Reference rs786203773(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131924535_131924536dupGA
CLNSRC
CLNACC RCV000167224.1,