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rs199476143

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199476143(A;A)
Make rs199476143(A;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position1606
GeneUGT1A12P
is asnp
is mentioned by
dbSNPrs199476143
ebirs199476143
HLIrs199476143
Exacrs199476143
Varsomers199476143
Maprs199476143
PheGenIrs199476143
hapmaprs199476143
1000 genomesrs199476143
hgdprs199476143
ensemblrs199476143
gopubmedrs199476143
geneviewrs199476143
scholarrs199476143
googlers199476143
pharmgkbrs199476143
gwascentralrs199476143
openSNPrs199476143
23andMers199476143
23andMe allrs199476143
SNP Nexus

SNPshotrs199476143
SNPdbers199476143
MSV3drs199476143
GWAS Ctlgrs199476143
Max Magnitude0
ClinVar
Risk rs199476143(A;A)
Alt rs199476143(A;A)
Reference Rs199476143(G;G)
Significance Pathogenic
Disease Ataxia
Variation info
Gene
CLNDBN Ataxia, progressive seizures, mental deterioration, and hearing loss
Reversed 0
HGVS NC_012920.1:m.1606G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010156.2,