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rs771887195

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771887195(-;-)
Make rs771887195(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108227667
GeneATM
is asnp
is mentioned by
dbSNPrs771887195
dbSNP (old)rs771887195
ClinGenrs771887195
ebirs771887195
HLIrs771887195
Exacrs771887195
Varsomers771887195
Maprs771887195
PheGenIrs771887195
Biobankrs771887195
1000 genomesrs771887195
hgdprs771887195
ensemblrs771887195
gopubmedrs771887195
geneviewrs771887195
scholarrs771887195
googlers771887195
pharmgkbrs771887195
gwascentralrs771887195
openSNPrs771887195
23andMers771887195
23andMe allrs771887195
SNP Nexus

SNPshotrs771887195
SNPdbers771887195
MSV3drs771887195
GWAS Ctlgrs771887195
Max Magnitude0
ClinVar
Risk rs771887195(-;-)
Alt rs771887195(-;-)
Reference Rs771887195(C;C)
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.108098394delC
CLNSRC
CLNACC RCV000223089.1, RCV000481023.1,