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rs775069541

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs775069541(G;G)
Make rs775069541(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132618277
GeneRAD50
is asnp
is mentioned by
dbSNPrs775069541
ClinGenrs775069541
ebirs775069541
HLIrs775069541
Exacrs775069541
Varsomers775069541
Maprs775069541
PheGenIrs775069541
hapmaprs775069541
1000 genomesrs775069541
hgdprs775069541
ensemblrs775069541
gopubmedrs775069541
geneviewrs775069541
scholarrs775069541
googlers775069541
pharmgkbrs775069541
gwascentralrs775069541
openSNPrs775069541
23andMers775069541
23andMe allrs775069541
SNP Nexus

SNPshotrs775069541
SNPdbers775069541
MSV3drs775069541
GWAS Ctlgrs775069541
Max Magnitude0
ClinVar
Risk rs775069541(A;A) rs775069541(G;G)
Alt rs775069541(A;A) rs775069541(G;G)
Reference Rs775069541(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131953969T>A
CLNSRC
CLNACC RCV000218193.1,