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rs774185390

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774185390(C;G)
Make rs774185390(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108227843
GeneATM
is asnp
is mentioned by
dbSNPrs774185390
ebirs774185390
HLIrs774185390
Exacrs774185390
Varsomers774185390
Maprs774185390
PheGenIrs774185390
hapmaprs774185390
1000 genomesrs774185390
hgdprs774185390
ensemblrs774185390
gopubmedrs774185390
geneviewrs774185390
scholarrs774185390
googlers774185390
pharmgkbrs774185390
gwascentralrs774185390
openSNPrs774185390
23andMers774185390
23andMe allrs774185390
SNP Nexus

SNPshotrs774185390
SNPdbers774185390
MSV3drs774185390
GWAS Ctlgrs774185390
Max Magnitude0
ClinVar
Risk rs774185390(G;G)
Alt rs774185390(G;G)
Reference rs774185390(C;C)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108098570C>G
CLNSRC
CLNACC RCV000196694.1,