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rs786202225

From SNPedia

Orientationplus
Geno Mag Summary
(ATCTC;ATCTC) 0 common in clinvar
Make rs786202225(-;-)
Make rs786202225(-;TCTCA)
Make rs786202225(TCTCA;TCTCA)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108235816
GeneATM
is asnp
is mentioned by
dbSNPrs786202225
ebirs786202225
HLIrs786202225
Exacrs786202225
Varsomers786202225
Maprs786202225
PheGenIrs786202225
hapmaprs786202225
1000 genomesrs786202225
hgdprs786202225
ensemblrs786202225
gopubmedrs786202225
geneviewrs786202225
scholarrs786202225
googlers786202225
pharmgkbrs786202225
gwascentralrs786202225
openSNPrs786202225
23andMers786202225
23andMe allrs786202225
SNP Nexus

SNPshotrs786202225
SNPdbers786202225
MSV3drs786202225
GWAS Ctlgrs786202225
Max Magnitude0
ClinVar
Risk rs786202225(;)
Alt rs786202225(;)
Reference rs786202225(ATCTC;ATCTC)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108106543_108106547delTCTCA
CLNSRC
CLNACC RCV000122852.1, RCV000164941.1,