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rs1057519364

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519364(G;T)
Make rs1057519364(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108253839
GeneATM
is asnp
is mentioned by
dbSNPrs1057519364
dbSNP (old)rs1057519364
ClinGenrs1057519364
ebirs1057519364
HLIrs1057519364
Exacrs1057519364
Gnomadrs1057519364
Varsomers1057519364
Maprs1057519364
PheGenIrs1057519364
Biobankrs1057519364
1000 genomesrs1057519364
hgdprs1057519364
ensemblrs1057519364
gopubmedrs1057519364
geneviewrs1057519364
scholarrs1057519364
googlers1057519364
pharmgkbrs1057519364
gwascentralrs1057519364
openSNPrs1057519364
23andMers1057519364
23andMe allrs1057519364
SNPshotrs1057519364
SNPdbers1057519364
MSV3drs1057519364
GWAS Ctlgrs1057519364
Max Magnitude0
ClinVar
Risk rs1057519364(T;T)
Alt rs1057519364(T;T)
Reference Rs1057519364(G;G)
Significance Probable-Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene ATM
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000011.9:g.108124566G>T
CLNSRC
CLNACC RCV000416923.1,