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rs786203370

From SNPedia

Orientationplus
Geno Mag Summary
(CATT;CATT) 0 common in clinvar
Make rs786203370(-;-)
Make rs786203370(-;TTCA)
Make rs786203370(TTCA;TTCA)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108227841
GeneATM
is asnp
is mentioned by
dbSNPrs786203370
ebirs786203370
HLIrs786203370
Exacrs786203370
Varsomers786203370
Maprs786203370
PheGenIrs786203370
hapmaprs786203370
1000 genomesrs786203370
hgdprs786203370
ensemblrs786203370
gopubmedrs786203370
geneviewrs786203370
scholarrs786203370
googlers786203370
pharmgkbrs786203370
gwascentralrs786203370
openSNPrs786203370
23andMers786203370
23andMe allrs786203370
SNP Nexus

SNPshotrs786203370
SNPdbers786203370
MSV3drs786203370
GWAS Ctlgrs786203370
Max Magnitude0
ClinVar
Risk rs786203370(;)
Alt rs786203370(;)
Reference rs786203370(CATT;CATT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108098568_108098571delTTCA
CLNSRC
CLNACC RCV000166647.1, RCV000235307.1,