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rs876660631

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660631(C;T)
Make rs876660631(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108229197
GeneATM
is asnp
is mentioned by
dbSNPrs876660631
ebirs876660631
HLIrs876660631
Exacrs876660631
Varsomers876660631
Maprs876660631
PheGenIrs876660631
hapmaprs876660631
1000 genomesrs876660631
hgdprs876660631
ensemblrs876660631
gopubmedrs876660631
geneviewrs876660631
scholarrs876660631
googlers876660631
pharmgkbrs876660631
gwascentralrs876660631
openSNPrs876660631
23andMers876660631
23andMe allrs876660631
SNP Nexus

SNPshotrs876660631
SNPdbers876660631
MSV3drs876660631
GWAS Ctlgrs876660631
Max Magnitude0
ClinVar
Risk rs876660631(T;T)
Alt rs876660631(T;T)
Reference rs876660631(C;C)
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.108099924C>T
CLNSRC
CLNACC RCV000213362.1,