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rs1060499575

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(GTGA;GTGA) 0 common in clinvar
Make rs1060499575(-;-)
Make rs1060499575(-;GTGA)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108343372
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs1060499575
dbSNP (old)rs1060499575
ClinGenrs1060499575
ebirs1060499575
HLIrs1060499575
Exacrs1060499575
Gnomadrs1060499575
Varsomers1060499575
Maprs1060499575
PheGenIrs1060499575
Biobankrs1060499575
1000 genomesrs1060499575
hgdprs1060499575
ensemblrs1060499575
gopubmedrs1060499575
geneviewrs1060499575
scholarrs1060499575
googlers1060499575
pharmgkbrs1060499575
gwascentralrs1060499575
openSNPrs1060499575
23andMers1060499575
23andMe allrs1060499575
SNPshotrs1060499575
SNPdbers1060499575
MSV3drs1060499575
GWAS Ctlgrs1060499575
Max Magnitude0
ClinVar
Risk rs1060499575(-;-)
Alt rs1060499575(-;-)
Reference Rs1060499575(GTGA;GTGA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108214103_108214106delGTGA
CLNSRC
CLNACC RCV000159624.5, RCV000204238.4, RCV000212083.2,