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rs778555849

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs778555849(C;T)
Make rs778555849(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132638158
GeneRAD50, TH2LCRR
is asnp
is mentioned by
dbSNPrs778555849
ebirs778555849
HLIrs778555849
Exacrs778555849
Varsomers778555849
Maprs778555849
PheGenIrs778555849
hapmaprs778555849
1000 genomesrs778555849
hgdprs778555849
ensemblrs778555849
gopubmedrs778555849
geneviewrs778555849
scholarrs778555849
googlers778555849
pharmgkbrs778555849
gwascentralrs778555849
openSNPrs778555849
23andMers778555849
23andMe allrs778555849
SNP Nexus

SNPshotrs778555849
SNPdbers778555849
MSV3drs778555849
GWAS Ctlgrs778555849
Max Magnitude0
ClinVar
Risk rs778555849(T;T)
Alt rs778555849(T;T)
Reference rs778555849(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene LOC101927761 TH2LCRR RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131973850C>T
CLNSRC
CLNACC RCV000199364.2,