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rs199731535

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199731535(A;A)
Make rs199731535(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position142549478
GeneATR
is asnp
is mentioned by
dbSNPrs199731535
dbSNP (old)rs199731535
ClinGenrs199731535
ebirs199731535
HLIrs199731535
Exacrs199731535
Gnomadrs199731535
Varsomers199731535
LitVarrs199731535
Maprs199731535
PheGenIrs199731535
Biobankrs199731535
1000 genomesrs199731535
hgdprs199731535
ensemblrs199731535
gopubmedrs199731535
geneviewrs199731535
scholarrs199731535
googlers199731535
pharmgkbrs199731535
gwascentralrs199731535
openSNPrs199731535
23andMers199731535
23andMe allrs199731535
SNPshotrs199731535
SNPdbers199731535
MSV3drs199731535
GWAS Ctlgrs199731535
Max Magnitude0
ClinVar
Risk rs199731535(A;A) rs199731535(T;T)
Alt rs199731535(A;A) rs199731535(T;T)
Reference Rs199731535(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATR
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.142268320C>T
CLNSRC
CLNACC RCV000434115.1,