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rs786203550

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786203550(C;G)
Make rs786203550(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108250889
GeneATM
is asnp
is mentioned by
dbSNPrs786203550
ebirs786203550
HLIrs786203550
Exacrs786203550
Varsomers786203550
Maprs786203550
PheGenIrs786203550
hapmaprs786203550
1000 genomesrs786203550
hgdprs786203550
ensemblrs786203550
gopubmedrs786203550
geneviewrs786203550
scholarrs786203550
googlers786203550
pharmgkbrs786203550
gwascentralrs786203550
openSNPrs786203550
23andMers786203550
23andMe allrs786203550
SNP Nexus

SNPshotrs786203550
SNPdbers786203550
MSV3drs786203550
GWAS Ctlgrs786203550
Max Magnitude0
ClinVar
Risk rs786203550(G;G)
Alt rs786203550(G;G)
Reference rs786203550(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108121616C>G
CLNSRC
CLNACC RCV000166909.1,