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

rs876660865

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660865(-;-)
Make rs876660865(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108284330
GeneATM
is asnp
is mentioned by
dbSNPrs876660865
ebirs876660865
HLIrs876660865
Exacrs876660865
Varsomers876660865
Maprs876660865
PheGenIrs876660865
hapmaprs876660865
1000 genomesrs876660865
hgdprs876660865
ensemblrs876660865
gopubmedrs876660865
geneviewrs876660865
scholarrs876660865
googlers876660865
pharmgkbrs876660865
gwascentralrs876660865
openSNPrs876660865
23andMers876660865
23andMe allrs876660865
SNP Nexus

SNPshotrs876660865
SNPdbers876660865
MSV3drs876660865
GWAS Ctlgrs876660865
Max Magnitude0
ClinVar
Risk rs876660865(;)
Alt rs876660865(;)
Reference rs876660865(A;A)
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.108155057delA
CLNSRC
CLNACC RCV000213614.1,