Have questions? Visit https://www.reddit.com/r/SNPedia

rs876660621

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660621(A;A)
Make rs876660621(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108281169
GeneATM
is asnp
is mentioned by
dbSNPrs876660621
ebirs876660621
HLIrs876660621
Exacrs876660621
Varsomers876660621
Maprs876660621
PheGenIrs876660621
hapmaprs876660621
1000 genomesrs876660621
hgdprs876660621
ensemblrs876660621
gopubmedrs876660621
geneviewrs876660621
scholarrs876660621
googlers876660621
pharmgkbrs876660621
gwascentralrs876660621
openSNPrs876660621
23andMers876660621
23andMe allrs876660621
SNP Nexus

SNPshotrs876660621
SNPdbers876660621
MSV3drs876660621
GWAS Ctlgrs876660621
Max Magnitude0
ClinVar
Risk rs876660621(A;A)
Alt rs876660621(A;A)
Reference rs876660621(G;G)
Significance Probable-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.108151896G>A
CLNSRC
CLNACC RCV000217092.1,