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rs786203734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs786203734(-;-)
Make rs786203734(-;TC)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108330371
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786203734
dbSNP (old)rs786203734
ClinGenrs786203734
ebirs786203734
HLIrs786203734
Exacrs786203734
Varsomers786203734
Maprs786203734
PheGenIrs786203734
Biobankrs786203734
1000 genomesrs786203734
hgdprs786203734
ensemblrs786203734
gopubmedrs786203734
geneviewrs786203734
scholarrs786203734
googlers786203734
pharmgkbrs786203734
gwascentralrs786203734
openSNPrs786203734
23andMers786203734
23andMe allrs786203734
SNP Nexus

SNPshotrs786203734
SNPdbers786203734
MSV3drs786203734
GWAS Ctlgrs786203734
Max Magnitude0
ClinVar
Risk rs786203734(-;-)
Alt rs786203734(-;-)
Reference Rs786203734(TC;TC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108201098_108201099delTC
CLNSRC
CLNACC RCV000167168.1,