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rs786202547

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs786202547(-;-)
Make rs786202547(-;GT)
Make rs786202547(GT;GT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108354859
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786202547
ebirs786202547
HLIrs786202547
Exacrs786202547
Varsomers786202547
Maprs786202547
PheGenIrs786202547
hapmaprs786202547
1000 genomesrs786202547
hgdprs786202547
ensemblrs786202547
gopubmedrs786202547
geneviewrs786202547
scholarrs786202547
googlers786202547
pharmgkbrs786202547
gwascentralrs786202547
openSNPrs786202547
23andMers786202547
23andMe allrs786202547
SNP Nexus

SNPshotrs786202547
SNPdbers786202547
MSV3drs786202547
GWAS Ctlgrs786202547
Max Magnitude0
ClinVar
Risk rs786202547(;)
Alt rs786202547(;)
Reference rs786202547(TG;TG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108225586_108225587delGT
CLNSRC
CLNACC RCV000165407.1,