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rs431905516

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs431905516(C;T)
Make rs431905516(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position1406226
GeneSLC6A3
is asnp
is mentioned by
dbSNPrs431905516
ebirs431905516
HLIrs431905516
Exacrs431905516
Varsomers431905516
Maprs431905516
PheGenIrs431905516
hapmaprs431905516
1000 genomesrs431905516
hgdprs431905516
ensemblrs431905516
gopubmedrs431905516
geneviewrs431905516
scholarrs431905516
googlers431905516
pharmgkbrs431905516
gwascentralrs431905516
openSNPrs431905516
23andMers431905516
23andMe allrs431905516
SNP Nexus

SNPshotrs431905516
SNPdbers431905516
MSV3drs431905516
GWAS Ctlgrs431905516
Max Magnitude0
ClinVar
Risk rs431905516(T;T)
Alt rs431905516(T;T)
Reference rs431905516(C;C)
Significance Pathogenic
Disease Infantile Parkinsonism-dystonia
Variation info
Gene SLC6A3
CLNDBN Infantile Parkinsonism-dystonia
Reversed 1
HGVS NC_000005.9:g.1406341G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000083264.3,