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rs587780624

From SNPedia

Orientationplus
Geno Mag Summary
(ATCTC;ATCTC) 0 common in clinvar
Make rs587780624(-;-)
Make rs587780624(-;ATCTC)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108235815
GeneATM
is asnp
is mentioned by
dbSNPrs587780624
ebirs587780624
HLIrs587780624
Exacrs587780624
Varsomers587780624
Maprs587780624
PheGenIrs587780624
hapmaprs587780624
1000 genomesrs587780624
hgdprs587780624
ensemblrs587780624
gopubmedrs587780624
geneviewrs587780624
scholarrs587780624
googlers587780624
pharmgkbrs587780624
gwascentralrs587780624
openSNPrs587780624
23andMers587780624
23andMe allrs587780624
SNP Nexus

SNPshotrs587780624
SNPdbers587780624
MSV3drs587780624
GWAS Ctlgrs587780624
Max Magnitude0
ClinVar
Risk rs587780624(;)
Alt rs587780624(;)
Reference rs587780624(ATCTC;ATCTC)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108106543_108106547delTCTCA
CLNSRC
CLNACC RCV000122852.1, RCV000164941.1,