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rs863224822

From SNPedia

Orientationplus
Make rs863224822(-;-)
Make rs863224822(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108254028
GeneATM
is asnp
is mentioned by
dbSNPrs863224822
ebirs863224822
HLIrs863224822
Exacrs863224822
Varsomers863224822
Maprs863224822
PheGenIrs863224822
hapmaprs863224822
1000 genomesrs863224822
hgdprs863224822
ensemblrs863224822
gopubmedrs863224822
geneviewrs863224822
scholarrs863224822
googlers863224822
pharmgkbrs863224822
gwascentralrs863224822
openSNPrs863224822
23andMers863224822
23andMe allrs863224822
SNP Nexus

SNPshotrs863224822
SNPdbers863224822
MSV3drs863224822
GWAS Ctlgrs863224822
Max Magnitude
ClinVar
Risk rs863224822(;)
Alt rs863224822(;)
Reference rs863224822(T;T)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108124755delT
CLNSRC
CLNACC RCV000199140.1,