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rs876658500

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658500(A;A)
Make rs876658500(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108235835
GeneATM
is asnp
is mentioned by
dbSNPrs876658500
ClinGenrs876658500
ebirs876658500
HLIrs876658500
Exacrs876658500
Varsomers876658500
Maprs876658500
PheGenIrs876658500
hapmaprs876658500
1000 genomesrs876658500
hgdprs876658500
ensemblrs876658500
gopubmedrs876658500
geneviewrs876658500
scholarrs876658500
googlers876658500
pharmgkbrs876658500
gwascentralrs876658500
openSNPrs876658500
23andMers876658500
23andMe allrs876658500
SNP Nexus

SNPshotrs876658500
SNPdbers876658500
MSV3drs876658500
GWAS Ctlgrs876658500
Max Magnitude0
ClinVar
Risk rs876658500(A;A)
Alt rs876658500(A;A)
Reference Rs876658500(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108106562G>A
CLNSRC
CLNACC RCV000220072.1,