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rs876658754

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658754(-;-)
Make rs876658754(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108244020
GeneATM
is asnp
is mentioned by
dbSNPrs876658754
ClinGenrs876658754
ebirs876658754
HLIrs876658754
Exacrs876658754
Varsomers876658754
Maprs876658754
PheGenIrs876658754
hapmaprs876658754
1000 genomesrs876658754
hgdprs876658754
ensemblrs876658754
gopubmedrs876658754
geneviewrs876658754
scholarrs876658754
googlers876658754
pharmgkbrs876658754
gwascentralrs876658754
openSNPrs876658754
23andMers876658754
23andMe allrs876658754
SNP Nexus

SNPshotrs876658754
SNPdbers876658754
MSV3drs876658754
GWAS Ctlgrs876658754
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs876658754(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108114747delT
CLNSRC
CLNACC RCV000215078.1,