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rs267607068

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607068(A;A)
Make rs267607068(A;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position1414744
GeneSLC6A3
is asnp
is mentioned by
dbSNPrs267607068
ebirs267607068
HLIrs267607068
Exacrs267607068
Varsomers267607068
Maprs267607068
PheGenIrs267607068
hapmaprs267607068
1000 genomesrs267607068
hgdprs267607068
ensemblrs267607068
gopubmedrs267607068
geneviewrs267607068
scholarrs267607068
googlers267607068
pharmgkbrs267607068
gwascentralrs267607068
openSNPrs267607068
23andMers267607068
23andMe allrs267607068
SNP Nexus

SNPshotrs267607068
SNPdbers267607068
MSV3drs267607068
GWAS Ctlgrs267607068
Max Magnitude0
ClinVar
Risk rs267607068(A;A)
Alt rs267607068(A;A)
Reference rs267607068(T;T)
Significance Pathogenic
Disease Infantile Parkinsonism-dystonia
Variation info
Gene SLC6A3
CLNDBN Infantile Parkinsonism-dystonia
Reversed 1
HGVS NC_000005.9:g.1414859A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018249.27,