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rs786204433

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204433(C;T)
Make rs786204433(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108304822
GeneATM
is asnp
is mentioned by
dbSNPrs786204433
ebirs786204433
HLIrs786204433
Exacrs786204433
Varsomers786204433
Maprs786204433
PheGenIrs786204433
hapmaprs786204433
1000 genomesrs786204433
hgdprs786204433
ensemblrs786204433
gopubmedrs786204433
geneviewrs786204433
scholarrs786204433
googlers786204433
pharmgkbrs786204433
gwascentralrs786204433
openSNPrs786204433
23andMers786204433
23andMe allrs786204433
SNP Nexus

SNPshotrs786204433
SNPdbers786204433
MSV3drs786204433
GWAS Ctlgrs786204433
Max Magnitude0
ClinVar
Risk rs786204433(T;T)
Alt rs786204433(T;T)
Reference rs786204433(C;C)
Significance Other
Disease Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000011.9:g.108175549C>T
CLNSRC
CLNACC RCV000169043.2, RCV000213135.1, RCV000235346.1,