rs121908622

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs121908622(A;A)

Make rs121908622(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

36234105

Gene

GNE

is a	snp
is	mentioned by
dbSNP	rs121908622
dbSNP (classic)	rs121908622
ClinGen	rs121908622
ebi	rs121908622
HLI	rs121908622
Exac	rs121908622
Gnomad	rs121908622
Varsome	rs121908622
LitVar	rs121908622
Map	rs121908622
PheGenI	rs121908622
Biobank	rs121908622
1000 genomes	rs121908622
hgdp	rs121908622
ensembl	rs121908622
geneview	rs121908622
scholar	rs121908622
google	rs121908622
pharmgkb	rs121908622
gwascentral	rs121908622
openSNP	rs121908622
23andMe	rs121908622
SNPshot	rs121908622
SNPdbe	rs121908622
MSV3d	rs121908622
GWAS Ctlg	rs121908622

Max Magnitude

0

OMIM	603824
Desc
Variant	0002
Related	also

OMIM	603824
Desc
Variant	0004
Related	also

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 UniProtKB (protein)
CLNACC	RCV000006393.3,