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rs876660134

From SNPedia

Orientationplus
Geno Mag Summary
(AAAGT;AAAGT) 0 common in clinvar
Make rs876660134(-;-)
Make rs876660134(-;TAAAG)
Make rs876660134(TAAAG;TAAAG)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108312471
GeneATM
is asnp
is mentioned by
dbSNPrs876660134
ebirs876660134
HLIrs876660134
Exacrs876660134
Varsomers876660134
Maprs876660134
PheGenIrs876660134
hapmaprs876660134
1000 genomesrs876660134
hgdprs876660134
ensemblrs876660134
gopubmedrs876660134
geneviewrs876660134
scholarrs876660134
googlers876660134
pharmgkbrs876660134
gwascentralrs876660134
openSNPrs876660134
23andMers876660134
23andMe allrs876660134
SNP Nexus

SNPshotrs876660134
SNPdbers876660134
MSV3drs876660134
GWAS Ctlgrs876660134
Max Magnitude0
ClinVar
Risk rs876660134(;)
Alt rs876660134(;)
Reference rs876660134(AAAGT;AAAGT)
Significance 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.108183198_108183202delTAAAG
CLNSRC
CLNACC RCV000219008.1,