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rs387906944

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906944(A;A)
Make rs387906944(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position75283509
GeneSLC25A19
is asnp
is mentioned by
dbSNPrs387906944
ebirs387906944
HLIrs387906944
Exacrs387906944
Varsomers387906944
Maprs387906944
PheGenIrs387906944
hapmaprs387906944
1000 genomesrs387906944
hgdprs387906944
ensemblrs387906944
gopubmedrs387906944
geneviewrs387906944
scholarrs387906944
googlers387906944
pharmgkbrs387906944
gwascentralrs387906944
openSNPrs387906944
23andMers387906944
23andMe allrs387906944
SNP Nexus

SNPshotrs387906944
SNPdbers387906944
MSV3drs387906944
GWAS Ctlgrs387906944
Max Magnitude0
ClinVar
Risk rs387906944(A;A)
Alt rs387906944(A;A)
Reference rs387906944(G;G)
Significance Pathogenic
Disease Striatal necrosis
Variation info
Gene SLC25A19
CLNDBN Striatal necrosis, bilateral, and progressive polyneuropathy
Reversed 1
HGVS NC_000017.10:g.73279590C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023554.2,