Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205213

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205213(-;-)
Make rs786205213(-;T)
Make rs786205213(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position227702244
GeneSLC19A3
is asnp
is mentioned by
dbSNPrs786205213
ebirs786205213
HLIrs786205213
Exacrs786205213
Varsomers786205213
Maprs786205213
PheGenIrs786205213
hapmaprs786205213
1000 genomesrs786205213
hgdprs786205213
ensemblrs786205213
gopubmedrs786205213
geneviewrs786205213
scholarrs786205213
googlers786205213
pharmgkbrs786205213
gwascentralrs786205213
openSNPrs786205213
23andMers786205213
23andMe allrs786205213
SNP Nexus

SNPshotrs786205213
SNPdbers786205213
MSV3drs786205213
GWAS Ctlgrs786205213
Max Magnitude0
ClinVar
Risk rs786205213(T;T)
Alt rs786205213(T;T)
Reference rs786205213(;)
Significance Pathogenic
Disease Basal ganglia disease
Variation info
Gene SLC19A3
CLNDBN Basal ganglia disease, biotin-responsive
Reversed 1
HGVS NC_000002.11:g.228566961dupA
CLNSRC
CLNACC RCV000170443.1,