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rs878854799

From SNPedia

Orientationplus
Geno Mag Summary
(AGAAATA;AGAAATA) 0 common in clinvar
Make rs878854799(-;-)
Make rs878854799(-;AGAAATA)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132638094
GeneRAD50, TH2LCRR
is asnp
is mentioned by
dbSNPrs878854799
ebirs878854799
HLIrs878854799
Exacrs878854799
Varsomers878854799
Maprs878854799
PheGenIrs878854799
hapmaprs878854799
1000 genomesrs878854799
hgdprs878854799
ensemblrs878854799
gopubmedrs878854799
geneviewrs878854799
scholarrs878854799
googlers878854799
pharmgkbrs878854799
gwascentralrs878854799
openSNPrs878854799
23andMers878854799
23andMe allrs878854799
SNP Nexus

SNPshotrs878854799
SNPdbers878854799
MSV3drs878854799
GWAS Ctlgrs878854799
Max Magnitude0
ClinVar
Risk rs878854799(;)
Alt rs878854799(;)
Reference rs878854799(AGAAATA;AGAAATA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TH2LCRR RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131973786_131973792delAGAAATA
CLNSRC
CLNACC RCV000226547.1,