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rs876660175

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 6 Breast cancer associated mutation
(G;G) 0 common in clinvar


Make rs876660175(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108301790
GeneATM
is asnp
is mentioned by
dbSNPrs876660175
dbSNP (classic)rs876660175
ClinGenrs876660175
ebirs876660175
HLIrs876660175
Exacrs876660175
Gnomadrs876660175
Varsomers876660175
LitVarrs876660175
Maprs876660175
PheGenIrs876660175
Biobankrs876660175
1000 genomesrs876660175
hgdprs876660175
ensemblrs876660175
geneviewrs876660175
scholarrs876660175
googlers876660175
pharmgkbrs876660175
gwascentralrs876660175
openSNPrs876660175
23andMers876660175
SNPshotrs876660175
SNPdbers876660175
MSV3drs876660175
GWAS Ctlgrs876660175
Max Magnitude6
ClinVar
Risk rs876660175(A;A) rs876660175(T;T)
Alt rs876660175(A;A) rs876660175(T;T)
Reference Rs876660175(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108172517G>A; NC_000011.9:g.108172517G>T
CLNSRC
CLNACC RCV000214126.1, RCV000411373.1,