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rs876659350

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659350(-;-)
Make rs876659350(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108333969
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876659350
ebirs876659350
HLIrs876659350
Exacrs876659350
Varsomers876659350
Maprs876659350
PheGenIrs876659350
hapmaprs876659350
1000 genomesrs876659350
hgdprs876659350
ensemblrs876659350
gopubmedrs876659350
geneviewrs876659350
scholarrs876659350
googlers876659350
pharmgkbrs876659350
gwascentralrs876659350
openSNPrs876659350
23andMers876659350
23andMe allrs876659350
SNP Nexus

SNPshotrs876659350
SNPdbers876659350
MSV3drs876659350
GWAS Ctlgrs876659350
Max Magnitude0
ClinVar
Risk rs876659350(;)
Alt rs876659350(;)
Reference rs876659350(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108204696delG
CLNSRC
CLNACC RCV000213901.1,