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rs786202259

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202259(-;-)
Make rs786202259(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132642204
GeneRAD50, TH2LCRR
is asnp
is mentioned by
dbSNPrs786202259
ebirs786202259
HLIrs786202259
Exacrs786202259
Varsomers786202259
Maprs786202259
PheGenIrs786202259
hapmaprs786202259
1000 genomesrs786202259
hgdprs786202259
ensemblrs786202259
gopubmedrs786202259
geneviewrs786202259
scholarrs786202259
googlers786202259
pharmgkbrs786202259
gwascentralrs786202259
openSNPrs786202259
23andMers786202259
23andMe allrs786202259
SNP Nexus

SNPshotrs786202259
SNPdbers786202259
MSV3drs786202259
GWAS Ctlgrs786202259
Max Magnitude0
ClinVar
Risk rs786202259(;)
Alt rs786202259(;)
Reference rs786202259(G;G)
Significance Other
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene LOC101927761 TH2LCRR RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131977896delG
CLNSRC
CLNACC RCV000164979.2,