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rs786203030

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs786203030(-;-)
Make rs786203030(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108354857
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786203030
ebirs786203030
HLIrs786203030
Exacrs786203030
Varsomers786203030
Maprs786203030
PheGenIrs786203030
hapmaprs786203030
1000 genomesrs786203030
hgdprs786203030
ensemblrs786203030
gopubmedrs786203030
geneviewrs786203030
scholarrs786203030
googlers786203030
pharmgkbrs786203030
gwascentralrs786203030
openSNPrs786203030
23andMers786203030
23andMe allrs786203030
SNP Nexus

SNPshotrs786203030
SNPdbers786203030
MSV3drs786203030
GWAS Ctlgrs786203030
Max Magnitude0
ClinVar
Risk rs786203030(;)
Alt rs786203030(;)
Reference rs786203030(CT;CT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108225584_108225585delCT
CLNSRC
CLNACC RCV000166157.1,