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rs121908621

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908621(C;T)
Make rs121908621(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position36234106
GeneGNE
is asnp
is mentioned by
dbSNPrs121908621
ebirs121908621
HLIrs121908621
Exacrs121908621
Varsomers121908621
Maprs121908621
PheGenIrs121908621
hapmaprs121908621
1000 genomesrs121908621
hgdprs121908621
ensemblrs121908621
gopubmedrs121908621
geneviewrs121908621
scholarrs121908621
googlers121908621
pharmgkbrs121908621
gwascentralrs121908621
openSNPrs121908621
23andMers121908621
23andMe allrs121908621
SNP Nexus

SNPshotrs121908621
SNPdbers121908621
MSV3drs121908621
GWAS Ctlgrs121908621
Max Magnitude0
OMIM603824
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908621(T;T)
Alt rs121908621(T;T)
Reference rs121908621(C;C)
Significance Pathogenic
Disease Sialuria
Variation info
Gene GNE
CLNDBN Sialuria
Reversed 1
HGVS NC_000009.11:g.36234103G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006392.2,