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

rs775539486

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs775539486(-;A)
Make rs775539486(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108327665
GeneATM
is asnp
is mentioned by
dbSNPrs775539486
ClinGenrs775539486
ebirs775539486
HLIrs775539486
Exacrs775539486
Varsomers775539486
Maprs775539486
PheGenIrs775539486
hapmaprs775539486
1000 genomesrs775539486
hgdprs775539486
ensemblrs775539486
gopubmedrs775539486
geneviewrs775539486
scholarrs775539486
googlers775539486
pharmgkbrs775539486
gwascentralrs775539486
openSNPrs775539486
23andMers775539486
23andMe allrs775539486
SNP Nexus

SNPshotrs775539486
SNPdbers775539486
MSV3drs775539486
GWAS Ctlgrs775539486
Max Magnitude0
ClinVar
Risk rs775539486(A;A)
Alt rs775539486(A;A)
Reference Rs775539486(;)
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.108198393dupA
CLNSRC
CLNACC RCV000129007.4, RCV000205392.2, RCV000236518.1,