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

rs864622163

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864622163(A;A)
Make rs864622163(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108244910
GeneATM
is asnp
is mentioned by
dbSNPrs864622163
ebirs864622163
HLIrs864622163
Exacrs864622163
Varsomers864622163
Maprs864622163
PheGenIrs864622163
hapmaprs864622163
1000 genomesrs864622163
hgdprs864622163
ensemblrs864622163
gopubmedrs864622163
geneviewrs864622163
scholarrs864622163
googlers864622163
pharmgkbrs864622163
gwascentralrs864622163
openSNPrs864622163
23andMers864622163
23andMe allrs864622163
SNP Nexus

SNPshotrs864622163
SNPdbers864622163
MSV3drs864622163
GWAS Ctlgrs864622163
Max Magnitude0
ClinVar
Risk rs864622163(A;A)
Alt rs864622163(A;A)
Reference rs864622163(T;T)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108115637T>A; NC_000011.9:g.108115637T>G
CLNSRC
CLNACC RCV000206320.1, RCV000223552.1,