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rs587781925

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781925(A;A)
Make rs587781925(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132638224
GeneRAD50, TH2LCRR
is asnp
is mentioned by
dbSNPrs587781925
ebirs587781925
HLIrs587781925
Exacrs587781925
Varsomers587781925
Maprs587781925
PheGenIrs587781925
hapmaprs587781925
1000 genomesrs587781925
hgdprs587781925
ensemblrs587781925
gopubmedrs587781925
geneviewrs587781925
scholarrs587781925
googlers587781925
pharmgkbrs587781925
gwascentralrs587781925
openSNPrs587781925
23andMers587781925
23andMe allrs587781925
SNP Nexus

SNPshotrs587781925
SNPdbers587781925
MSV3drs587781925
GWAS Ctlgrs587781925
Max Magnitude0
ClinVar
Risk rs587781925(A;A)
Alt rs587781925(A;A)
Reference rs587781925(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene LOC101927761 TH2LCRR RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131973916G>A
CLNSRC
CLNACC RCV000130277.2,