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rs758654836

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs758654836(C;C)
Make rs758654836(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108335958
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs758654836
ebirs758654836
HLIrs758654836
Exacrs758654836
Varsomers758654836
Maprs758654836
PheGenIrs758654836
hapmaprs758654836
1000 genomesrs758654836
hgdprs758654836
ensemblrs758654836
gopubmedrs758654836
geneviewrs758654836
scholarrs758654836
googlers758654836
pharmgkbrs758654836
gwascentralrs758654836
openSNPrs758654836
23andMers758654836
23andMe allrs758654836
SNP Nexus

SNPshotrs758654836
SNPdbers758654836
MSV3drs758654836
GWAS Ctlgrs758654836
Max Magnitude0
ClinVar
Risk rs758654836(C;C)
Alt rs758654836(C;C)
Reference rs758654836(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000011.9:g.108206685T>C; NC_000011.9:g.108206685T>G
CLNSRC
CLNACC RCV000221847.1, RCV000237049.1,