Have questions? Visit https://www.reddit.com/r/SNPedia

rs786203421

From SNPedia

Orientationplus
Geno Mag Summary
(TACA;TACA) 0 common in clinvar
Make rs786203421(-;-)
Make rs786203421(-;TACA)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108327669
GeneATM
is asnp
is mentioned by
dbSNPrs786203421
ebirs786203421
HLIrs786203421
Exacrs786203421
Varsomers786203421
Maprs786203421
PheGenIrs786203421
hapmaprs786203421
1000 genomesrs786203421
hgdprs786203421
ensemblrs786203421
gopubmedrs786203421
geneviewrs786203421
scholarrs786203421
googlers786203421
pharmgkbrs786203421
gwascentralrs786203421
openSNPrs786203421
23andMers786203421
23andMe allrs786203421
SNP Nexus

SNPshotrs786203421
SNPdbers786203421
MSV3drs786203421
GWAS Ctlgrs786203421
Max Magnitude0
ClinVar
Risk rs786203421(;)
Alt rs786203421(;)
Reference rs786203421(TACA;TACA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108198396_108198399delTACA
CLNSRC
CLNACC RCV000166719.1, RCV000232032.1,