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rs786202695

From SNPedia

Orientationplus
Geno Mag Summary
(TGTG;TGTG) 0 common in clinvar
Make rs786202695(-;-)
Make rs786202695(-;GTGT)
Make rs786202695(GTGT;GTGT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108268491
GeneATM
is asnp
is mentioned by
dbSNPrs786202695
ebirs786202695
HLIrs786202695
Exacrs786202695
Varsomers786202695
Maprs786202695
PheGenIrs786202695
hapmaprs786202695
1000 genomesrs786202695
hgdprs786202695
ensemblrs786202695
gopubmedrs786202695
geneviewrs786202695
scholarrs786202695
googlers786202695
pharmgkbrs786202695
gwascentralrs786202695
openSNPrs786202695
23andMers786202695
23andMe allrs786202695
SNP Nexus

SNPshotrs786202695
SNPdbers786202695
MSV3drs786202695
GWAS Ctlgrs786202695
Max Magnitude0
ClinVar
Risk rs786202695(;)
Alt rs786202695(;)
Reference rs786202695(TGTG;TGTG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108139218_108139221delGTGT
CLNSRC
CLNACC RCV000165633.1, RCV000193120.2,