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rs786203501

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203501(-;-)
Make rs786203501(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108284375
GeneATM
is asnp
is mentioned by
dbSNPrs786203501
ebirs786203501
HLIrs786203501
Exacrs786203501
Varsomers786203501
Maprs786203501
PheGenIrs786203501
hapmaprs786203501
1000 genomesrs786203501
hgdprs786203501
ensemblrs786203501
gopubmedrs786203501
geneviewrs786203501
scholarrs786203501
googlers786203501
pharmgkbrs786203501
gwascentralrs786203501
openSNPrs786203501
23andMers786203501
23andMe allrs786203501
SNP Nexus

SNPshotrs786203501
SNPdbers786203501
MSV3drs786203501
GWAS Ctlgrs786203501
Max Magnitude0
ClinVar
Risk rs786203501(;)
Alt rs786203501(;)
Reference rs786203501(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.108155102delG
CLNSRC
CLNACC RCV000166833.1,