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rs876660175

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660175(A;A)
Make rs876660175(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108301790
GeneATM
is asnp
is mentioned by
dbSNPrs876660175
ebirs876660175
HLIrs876660175
Exacrs876660175
Varsomers876660175
Maprs876660175
PheGenIrs876660175
hapmaprs876660175
1000 genomesrs876660175
hgdprs876660175
ensemblrs876660175
gopubmedrs876660175
geneviewrs876660175
scholarrs876660175
googlers876660175
pharmgkbrs876660175
gwascentralrs876660175
openSNPrs876660175
23andMers876660175
23andMe allrs876660175
SNP Nexus

SNPshotrs876660175
SNPdbers876660175
MSV3drs876660175
GWAS Ctlgrs876660175
Max Magnitude0
ClinVar
Risk rs876660175(A;A)
Alt rs876660175(A;A)
Reference rs876660175(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.108172517G>A
CLNSRC
CLNACC RCV000214126.1,