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rs376603775

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376603775(C;T)
Make rs376603775(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108304801
GeneATM
is asnp
is mentioned by
dbSNPrs376603775
ebirs376603775
HLIrs376603775
Exacrs376603775
Varsomers376603775
Maprs376603775
PheGenIrs376603775
hapmaprs376603775
1000 genomesrs376603775
hgdprs376603775
ensemblrs376603775
gopubmedrs376603775
geneviewrs376603775
scholarrs376603775
googlers376603775
pharmgkbrs376603775
gwascentralrs376603775
openSNPrs376603775
23andMers376603775
23andMe allrs376603775
SNP Nexus

SNPshotrs376603775
SNPdbers376603775
MSV3drs376603775
GWAS Ctlgrs376603775
Max Magnitude0
ClinVar
Risk rs376603775(T;T)
Alt rs376603775(T;T)
Reference rs376603775(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ATM
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.108175528C>T
CLNSRC
CLNACC RCV000236653.1,