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

rs786202187

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202187(-;-)
Make rs786202187(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132618114
GeneRAD50
is asnp
is mentioned by
dbSNPrs786202187
ebirs786202187
HLIrs786202187
Exacrs786202187
Varsomers786202187
Maprs786202187
PheGenIrs786202187
hapmaprs786202187
1000 genomesrs786202187
hgdprs786202187
ensemblrs786202187
gopubmedrs786202187
geneviewrs786202187
scholarrs786202187
googlers786202187
pharmgkbrs786202187
gwascentralrs786202187
openSNPrs786202187
23andMers786202187
23andMe allrs786202187
SNP Nexus

SNPshotrs786202187
SNPdbers786202187
MSV3drs786202187
GWAS Ctlgrs786202187
Max Magnitude0
ClinVar
Risk rs786202187(;)
Alt rs786202187(;)
Reference rs786202187(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131953806delA
CLNSRC
CLNACC RCV000164886.1,