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rs778269655

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs778269655(A;A)
Make rs778269655(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108343260
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs778269655
ebirs778269655
HLIrs778269655
Exacrs778269655
Varsomers778269655
Maprs778269655
PheGenIrs778269655
hapmaprs778269655
1000 genomesrs778269655
hgdprs778269655
ensemblrs778269655
gopubmedrs778269655
geneviewrs778269655
scholarrs778269655
googlers778269655
pharmgkbrs778269655
gwascentralrs778269655
openSNPrs778269655
23andMers778269655
23andMe allrs778269655
SNP Nexus

SNPshotrs778269655
SNPdbers778269655
MSV3drs778269655
GWAS Ctlgrs778269655
Max Magnitude0
ClinVar
Risk rs778269655(A;A)
Alt rs778269655(A;A)
Reference rs778269655(G;G)
Significance Other
Disease Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108213987G>A
CLNSRC
CLNACC RCV000169516.2,