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rs786203539

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786203539(-;-)
Make rs786203539(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108271294
GeneATM
is asnp
is mentioned by
dbSNPrs786203539
ebirs786203539
HLIrs786203539
Exacrs786203539
Varsomers786203539
Maprs786203539
PheGenIrs786203539
hapmaprs786203539
1000 genomesrs786203539
hgdprs786203539
ensemblrs786203539
gopubmedrs786203539
geneviewrs786203539
scholarrs786203539
googlers786203539
pharmgkbrs786203539
gwascentralrs786203539
openSNPrs786203539
23andMers786203539
23andMe allrs786203539
SNP Nexus

SNPshotrs786203539
SNPdbers786203539
MSV3drs786203539
GWAS Ctlgrs786203539
Max Magnitude0
ClinVar
Risk rs786203539(;)
Alt rs786203539(;)
Reference rs786203539(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108142021delA
CLNSRC
CLNACC RCV000166890.1,