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rs786203976

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs786203976(-;-)
Make rs786203976(-;TCT)
Make rs786203976(TCT;TCT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108345902
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786203976
ClinGenrs786203976
ebirs786203976
HLIrs786203976
Exacrs786203976
Varsomers786203976
Maprs786203976
PheGenIrs786203976
hapmaprs786203976
1000 genomesrs786203976
hgdprs786203976
ensemblrs786203976
gopubmedrs786203976
geneviewrs786203976
scholarrs786203976
googlers786203976
pharmgkbrs786203976
gwascentralrs786203976
openSNPrs786203976
23andMers786203976
23andMe allrs786203976
SNP Nexus

SNPshotrs786203976
SNPdbers786203976
MSV3drs786203976
GWAS Ctlgrs786203976
Max Magnitude0
ClinVar
Risk rs786203976(-;-)
Alt rs786203976(-;-)
Reference Rs786203976(CTT;CTT)
Significance Other
Disease Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not specified
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000011.9:g.108216629_108216631delTCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000003154.3, RCV000167512.2, RCV000480186.1,