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rs786204088

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204088(A;A)
Make rs786204088(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108227697
GeneATM
is asnp
is mentioned by
dbSNPrs786204088
ebirs786204088
HLIrs786204088
Exacrs786204088
Varsomers786204088
Maprs786204088
PheGenIrs786204088
hapmaprs786204088
1000 genomesrs786204088
hgdprs786204088
ensemblrs786204088
gopubmedrs786204088
geneviewrs786204088
scholarrs786204088
googlers786204088
pharmgkbrs786204088
gwascentralrs786204088
openSNPrs786204088
23andMers786204088
23andMe allrs786204088
SNP Nexus

SNPshotrs786204088
SNPdbers786204088
MSV3drs786204088
GWAS Ctlgrs786204088
Max Magnitude0
ClinVar
Risk rs786204088(A;A)
Alt rs786204088(A;A)
Reference rs786204088(G;G)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108098424G>A
CLNSRC
CLNACC RCV000167987.1,