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rs398122819

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398122819(-;-)
Make rs398122819(-;A)
ReferenceGRCh38 38.1/141
Chromosome6
Position56476257
GeneDST
is asnp
is mentioned by
dbSNPrs398122819
ebirs398122819
HLIrs398122819
Exacrs398122819
Varsomers398122819
Maprs398122819
PheGenIrs398122819
hapmaprs398122819
1000 genomesrs398122819
hgdprs398122819
ensemblrs398122819
gopubmedrs398122819
geneviewrs398122819
scholarrs398122819
googlers398122819
pharmgkbrs398122819
gwascentralrs398122819
openSNPrs398122819
23andMers398122819
23andMe allrs398122819
SNP Nexus

SNPshotrs398122819
SNPdbers398122819
MSV3drs398122819
GWAS Ctlgrs398122819
Max Magnitude0
ClinVar
Risk rs398122819(;)
Alt rs398122819(;)
Reference rs398122819(A;A)
Significance Pathogenic
Disease Neuropathy
Variation info
Gene DST
CLNDBN Neuropathy, hereditary sensory and autonomic, type VI
Reversed 1
HGVS NC_000006.11:g.56341055delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000024316.29,