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rs200976093

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200976093(C;T)
Make rs200976093(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position108284411
GeneATM
is asnp
is mentioned by
dbSNPrs200976093
ebirs200976093
HLIrs200976093
Exacrs200976093
Varsomers200976093
Maprs200976093
PheGenIrs200976093
hapmaprs200976093
1000 genomesrs200976093
hgdprs200976093
ensemblrs200976093
gopubmedrs200976093
geneviewrs200976093
scholarrs200976093
googlers200976093
pharmgkbrs200976093
gwascentralrs200976093
openSNPrs200976093
23andMers200976093
23andMe allrs200976093
SNP Nexus

SNPshotrs200976093
SNPdbers200976093
MSV3drs200976093
GWAS Ctlgrs200976093
Max Magnitude0
ClinVar
Risk rs200976093(T;T)
Alt rs200976093(T;T)
Reference rs200976093(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ATM
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.108155138C>T
CLNSRC ClinVar GeneDx
CLNACC RCV000115183.2,