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rs121908622

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908622(A;A)
Make rs121908622(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position36234105
GeneGNE
is asnp
is mentioned by
dbSNPrs121908622
ebirs121908622
HLIrs121908622
Exacrs121908622
Varsomers121908622
Maprs121908622
PheGenIrs121908622
hapmaprs121908622
1000 genomesrs121908622
hgdprs121908622
ensemblrs121908622
gopubmedrs121908622
geneviewrs121908622
scholarrs121908622
googlers121908622
pharmgkbrs121908622
gwascentralrs121908622
openSNPrs121908622
23andMers121908622
23andMe allrs121908622
SNP Nexus

SNPshotrs121908622
SNPdbers121908622
MSV3drs121908622
GWAS Ctlgrs121908622
Max Magnitude0
OMIM603824
Desc
Variant0002
Relatedalso
OMIM603824
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908622(A;A)
Alt rs121908622(A;A)
Reference rs121908622(G;G)
Significance Pathogenic
Disease Sialuria
Variation info
Gene GNE
CLNDBN Sialuria
Reversed 1
HGVS NC_000009.11:g.36234102C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006393.3,