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rs786201897

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786201897(-;-)
Make rs786201897(-;A)
Make rs786201897(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132604039
GeneRAD50
is asnp
is mentioned by
dbSNPrs786201897
ebirs786201897
HLIrs786201897
Exacrs786201897
Varsomers786201897
Maprs786201897
PheGenIrs786201897
hapmaprs786201897
1000 genomesrs786201897
hgdprs786201897
ensemblrs786201897
gopubmedrs786201897
geneviewrs786201897
scholarrs786201897
googlers786201897
pharmgkbrs786201897
gwascentralrs786201897
openSNPrs786201897
23andMers786201897
23andMe allrs786201897
SNP Nexus

SNPshotrs786201897
SNPdbers786201897
MSV3drs786201897
GWAS Ctlgrs786201897
Max Magnitude0
ClinVar
Risk rs786201897(A;A)
Alt rs786201897(A;A)
Reference rs786201897(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131939731dupA
CLNSRC
CLNACC RCV000164416.1,