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rs876660743

From SNPedia

Orientationplus
Geno Mag Summary
(TGT;TGT) 0 common in clinvar
Make rs876660743(-;-)
Make rs876660743(-;TGT)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108333947
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876660743
ebirs876660743
HLIrs876660743
Exacrs876660743
Varsomers876660743
Maprs876660743
PheGenIrs876660743
hapmaprs876660743
1000 genomesrs876660743
hgdprs876660743
ensemblrs876660743
gopubmedrs876660743
geneviewrs876660743
scholarrs876660743
googlers876660743
pharmgkbrs876660743
gwascentralrs876660743
openSNPrs876660743
23andMers876660743
23andMe allrs876660743
SNP Nexus

SNPshotrs876660743
SNPdbers876660743
MSV3drs876660743
GWAS Ctlgrs876660743
Max Magnitude0
ClinVar
Risk rs876660743(;)
Alt rs876660743(;)
Reference rs876660743(TGT;TGT)
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.108204674_108204676delTGT
CLNSRC
CLNACC RCV000214450.1,