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rs587782525

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782525(-;-)
Make rs587782525(-;AA)
Make rs587782525(AA;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108335898
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587782525
ebirs587782525
HLIrs587782525
Exacrs587782525
Varsomers587782525
Maprs587782525
PheGenIrs587782525
hapmaprs587782525
1000 genomesrs587782525
hgdprs587782525
ensemblrs587782525
gopubmedrs587782525
geneviewrs587782525
scholarrs587782525
googlers587782525
pharmgkbrs587782525
gwascentralrs587782525
openSNPrs587782525
23andMers587782525
23andMe allrs587782525
SNP Nexus

SNPshotrs587782525
SNPdbers587782525
MSV3drs587782525
GWAS Ctlgrs587782525
Max Magnitude0
ClinVar
Risk rs587782525(TAA,TGT;TAA,TGT)
Alt rs587782525(TAA,TGT;TAA,TGT)
Reference rs587782525(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108206624_108206625dupGT; NC_000011.9:g.108206625_108206626insAA
CLNSRC
CLNACC RCV000215590.1, RCV000131713.2,