rs121908623

Orientation

minus

Stabilized

minus

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

Make rs121908623(G;T)

Make rs121908623(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

36234114

Gene

GNE

is a	snp
is	mentioned by
dbSNP	rs121908623
dbSNP (classic)	rs121908623
ClinGen	rs121908623
ebi	rs121908623
HLI	rs121908623
Exac	rs121908623
Gnomad	rs121908623
Varsome	rs121908623
LitVar	rs121908623
Map	rs121908623
PheGenI	rs121908623
Biobank	rs121908623
1000 genomes	rs121908623
hgdp	rs121908623
ensembl	rs121908623
geneview	rs121908623
scholar	rs121908623
google	rs121908623
pharmgkb	rs121908623
gwascentral	rs121908623
openSNP	rs121908623
23andMe	rs121908623
SNPshot	rs121908623
SNPdbe	rs121908623
MSV3d	rs121908623
GWAS Ctlg	rs121908623

Max Magnitude

0

OMIM	603824
Desc
Variant	0003
Related	also

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 UniProtKB (protein)
CLNACC	RCV000006394.2,