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rs752135143

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs752135143(A;A)
Make rs752135143(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108229328
GeneATM
is asnp
is mentioned by
dbSNPrs752135143
ebirs752135143
HLIrs752135143
Exacrs752135143
Varsomers752135143
Maprs752135143
PheGenIrs752135143
hapmaprs752135143
1000 genomesrs752135143
hgdprs752135143
ensemblrs752135143
gopubmedrs752135143
geneviewrs752135143
scholarrs752135143
googlers752135143
pharmgkbrs752135143
gwascentralrs752135143
openSNPrs752135143
23andMers752135143
23andMe allrs752135143
SNP Nexus

SNPshotrs752135143
SNPdbers752135143
MSV3drs752135143
GWAS Ctlgrs752135143
Max Magnitude0
ClinVar
Risk rs752135143(A;A)
Alt rs752135143(A;A)
Reference rs752135143(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108100055G>A
CLNSRC
CLNACC RCV000216445.1,