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rs750586158

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs750586158(C;T)
Make rs750586158(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132638203
GeneRAD50, TH2LCRR
is asnp
is mentioned by
dbSNPrs750586158
ebirs750586158
HLIrs750586158
Exacrs750586158
Varsomers750586158
Maprs750586158
PheGenIrs750586158
hapmaprs750586158
1000 genomesrs750586158
hgdprs750586158
ensemblrs750586158
gopubmedrs750586158
geneviewrs750586158
scholarrs750586158
googlers750586158
pharmgkbrs750586158
gwascentralrs750586158
openSNPrs750586158
23andMers750586158
23andMe allrs750586158
SNP Nexus

SNPshotrs750586158
SNPdbers750586158
MSV3drs750586158
GWAS Ctlgrs750586158
Max Magnitude0
ClinVar
Risk rs750586158(T;T)
Alt rs750586158(T;T)
Reference rs750586158(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.131973895C>T
CLNSRC
CLNACC RCV000164215.2,