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rs786202418

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202418(A;TT)
Make rs786202418(TT;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108343320
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786202418
ebirs786202418
HLIrs786202418
Exacrs786202418
Varsomers786202418
Maprs786202418
PheGenIrs786202418
hapmaprs786202418
1000 genomesrs786202418
hgdprs786202418
ensemblrs786202418
gopubmedrs786202418
geneviewrs786202418
scholarrs786202418
googlers786202418
pharmgkbrs786202418
gwascentralrs786202418
openSNPrs786202418
23andMers786202418
23andMe allrs786202418
SNP Nexus

SNPshotrs786202418
SNPdbers786202418
MSV3drs786202418
GWAS Ctlgrs786202418
Max Magnitude0
ClinVar
Risk rs786202418(TT;TT)
Alt rs786202418(TT;TT)
Reference rs786202418(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108214047delAinsTT
CLNSRC
CLNACC RCV000165220.1,