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rs876658832

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs876658832(-;-)
Make rs876658832(-;TA)
Make rs876658832(TA;TA)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108247039
GeneATM
is asnp
is mentioned by
dbSNPrs876658832
ClinGenrs876658832
ebirs876658832
HLIrs876658832
Exacrs876658832
Varsomers876658832
Maprs876658832
PheGenIrs876658832
hapmaprs876658832
1000 genomesrs876658832
hgdprs876658832
ensemblrs876658832
gopubmedrs876658832
geneviewrs876658832
scholarrs876658832
googlers876658832
pharmgkbrs876658832
gwascentralrs876658832
openSNPrs876658832
23andMers876658832
23andMe allrs876658832
SNP Nexus

SNPshotrs876658832
SNPdbers876658832
MSV3drs876658832
GWAS Ctlgrs876658832
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs876658832(AT;AT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108117766_108117767delTA
CLNSRC
CLNACC RCV000216433.1,