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rs747855862

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs747855862(A;A)
Make rs747855862(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108235669
GeneATM
is asnp
is mentioned by
dbSNPrs747855862
dbSNP (old)rs747855862
ClinGenrs747855862
ebirs747855862
HLIrs747855862
Exacrs747855862
Gnomadrs747855862
Varsomers747855862
Maprs747855862
PheGenIrs747855862
Biobankrs747855862
1000 genomesrs747855862
hgdprs747855862
ensemblrs747855862
gopubmedrs747855862
geneviewrs747855862
scholarrs747855862
googlers747855862
pharmgkbrs747855862
gwascentralrs747855862
openSNPrs747855862
23andMers747855862
23andMe allrs747855862
SNP Nexus

SNPshotrs747855862
SNPdbers747855862
MSV3drs747855862
GWAS Ctlgrs747855862
Max Magnitude0
ClinVar
Risk rs747855862(A;A)
Alt rs747855862(A;A)
Reference Rs747855862(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108106396G>A
CLNSRC
CLNACC RCV000217634.1, RCV000480467.1,