Have questions? Visit https://www.reddit.com/r/SNPedia

rs876660041

From SNPedia

Orientationplus
Geno Mag Summary
(TAATG;TAATG) 0 common in clinvar
Make rs876660041(-;-)
Make rs876660041(-;TGTAA)
Make rs876660041(TGTAA;TGTAA)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108331557
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876660041
ebirs876660041
HLIrs876660041
Exacrs876660041
Varsomers876660041
Maprs876660041
PheGenIrs876660041
hapmaprs876660041
1000 genomesrs876660041
hgdprs876660041
ensemblrs876660041
gopubmedrs876660041
geneviewrs876660041
scholarrs876660041
googlers876660041
pharmgkbrs876660041
gwascentralrs876660041
openSNPrs876660041
23andMers876660041
23andMe allrs876660041
SNP Nexus

SNPshotrs876660041
SNPdbers876660041
MSV3drs876660041
GWAS Ctlgrs876660041
Max Magnitude0
ClinVar
Risk rs876660041(;)
Alt rs876660041(;)
Reference rs876660041(TAATG;TAATG)
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.108202284_108202288delTGTAA
CLNSRC
CLNACC RCV000219911.1,