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rs1057520672

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520672(C;T)
Make rs1057520672(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108347335
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs1057520672
dbSNP (old)rs1057520672
ClinGenrs1057520672
ebirs1057520672
HLIrs1057520672
Exacrs1057520672
Gnomadrs1057520672
Varsomers1057520672
LitVarrs1057520672
Maprs1057520672
PheGenIrs1057520672
Biobankrs1057520672
1000 genomesrs1057520672
hgdprs1057520672
ensemblrs1057520672
gopubmedrs1057520672
geneviewrs1057520672
scholarrs1057520672
googlers1057520672
pharmgkbrs1057520672
gwascentralrs1057520672
openSNPrs1057520672
23andMers1057520672
23andMe allrs1057520672
SNPshotrs1057520672
SNPdbers1057520672
MSV3drs1057520672
GWAS Ctlgrs1057520672
Max Magnitude0
ClinVar
Risk rs1057520672(T;T)
Alt rs1057520672(T;T)
Reference Rs1057520672(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene C11orf65 ATM
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.108218062C>T
CLNSRC
CLNACC RCV000421983.1,