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rs786203491

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786203491(-;-)
Make rs786203491(-;A)
Make rs786203491(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108345756
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786203491
ebirs786203491
HLIrs786203491
Exacrs786203491
Varsomers786203491
Maprs786203491
PheGenIrs786203491
hapmaprs786203491
1000 genomesrs786203491
hgdprs786203491
ensemblrs786203491
gopubmedrs786203491
geneviewrs786203491
scholarrs786203491
googlers786203491
pharmgkbrs786203491
gwascentralrs786203491
openSNPrs786203491
23andMers786203491
23andMe allrs786203491
SNP Nexus

SNPshotrs786203491
SNPdbers786203491
MSV3drs786203491
GWAS Ctlgrs786203491
Max Magnitude0
ClinVar
Risk rs786203491(A;A)
Alt rs786203491(A;A)
Reference rs786203491(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108216483dupA
CLNSRC
CLNACC RCV000166814.1,