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rs587781717

From SNPedia

Orientationplus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs587781717(-;-)
Make rs587781717(-;GAAA)
Make rs587781717(GAAA;GAAA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108247089
GeneATM
is asnp
is mentioned by
dbSNPrs587781717
ebirs587781717
HLIrs587781717
Exacrs587781717
Varsomers587781717
Maprs587781717
PheGenIrs587781717
hapmaprs587781717
1000 genomesrs587781717
hgdprs587781717
ensemblrs587781717
gopubmedrs587781717
geneviewrs587781717
scholarrs587781717
googlers587781717
pharmgkbrs587781717
gwascentralrs587781717
openSNPrs587781717
23andMers587781717
23andMe allrs587781717
SNP Nexus

SNPshotrs587781717
SNPdbers587781717
MSV3drs587781717
GWAS Ctlgrs587781717
Max Magnitude0
ClinVar
Risk rs587781717(;)
Alt rs587781717(;)
Reference rs587781717(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,