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rs587780612

From SNPedia

Orientationplus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs587780612(-;-)
Make rs587780612(-;AAAG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108247086
GeneATM
is asnp
is mentioned by
dbSNPrs587780612
ebirs587780612
HLIrs587780612
Exacrs587780612
Varsomers587780612
Maprs587780612
PheGenIrs587780612
hapmaprs587780612
1000 genomesrs587780612
hgdprs587780612
ensemblrs587780612
gopubmedrs587780612
geneviewrs587780612
scholarrs587780612
googlers587780612
pharmgkbrs587780612
gwascentralrs587780612
openSNPrs587780612
23andMers587780612
23andMe allrs587780612
SNP Nexus

SNPshotrs587780612
SNPdbers587780612
MSV3drs587780612
GWAS Ctlgrs587780612
Max Magnitude0
ClinVar
Risk rs587780612(;)
Alt rs587780612(;)
Reference rs587780612(AAAG;AAAG)
Significance Other
Disease Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108117816_108117819delGAAA
CLNSRC Ambry Genetics Counsyl
CLNACC RCV000122816.6, RCV000129901.3, RCV000236560.1,