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rs121908623

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908623(G;T)
Make rs121908623(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position36234114
GeneGNE
is asnp
is mentioned by
dbSNPrs121908623
ebirs121908623
HLIrs121908623
Exacrs121908623
Varsomers121908623
Maprs121908623
PheGenIrs121908623
hapmaprs121908623
1000 genomesrs121908623
hgdprs121908623
ensemblrs121908623
gopubmedrs121908623
geneviewrs121908623
scholarrs121908623
googlers121908623
pharmgkbrs121908623
gwascentralrs121908623
openSNPrs121908623
23andMers121908623
23andMe allrs121908623
SNP Nexus

SNPshotrs121908623
SNPdbers121908623
MSV3drs121908623
GWAS Ctlgrs121908623
Max Magnitude0
OMIM603824
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908623(T;T)
Alt rs121908623(T;T)
Reference rs121908623(G;G)
Significance Pathogenic
Disease Sialuria
Variation info
Gene GNE
CLNDBN Sialuria
Reversed 1
HGVS NC_000009.11:g.36234111C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006394.2,