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rs786203507

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203507(-;-)
Make rs786203507(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108284240
GeneATM
is asnp
is mentioned by
dbSNPrs786203507
ebirs786203507
HLIrs786203507
Exacrs786203507
Varsomers786203507
Maprs786203507
PheGenIrs786203507
hapmaprs786203507
1000 genomesrs786203507
hgdprs786203507
ensemblrs786203507
gopubmedrs786203507
geneviewrs786203507
scholarrs786203507
googlers786203507
pharmgkbrs786203507
gwascentralrs786203507
openSNPrs786203507
23andMers786203507
23andMe allrs786203507
SNP Nexus

SNPshotrs786203507
SNPdbers786203507
MSV3drs786203507
GWAS Ctlgrs786203507
Max Magnitude0
ClinVar
Risk rs786203507(;)
Alt rs786203507(;)
Reference rs786203507(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108154967delG
CLNSRC
CLNACC RCV000166841.1,