rs104893981

Orientation

minus

Stabilized

minus

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

Make rs104893981(C;T)

Make rs104893981(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31860170

Gene

NEU1

is a	snp
is	mentioned by
dbSNP	rs104893981
dbSNP (classic)	rs104893981
ClinGen	rs104893981
ebi	rs104893981
HLI	rs104893981
Exac	rs104893981
Gnomad	rs104893981
Varsome	rs104893981
LitVar	rs104893981
Map	rs104893981
PheGenI	rs104893981
Biobank	rs104893981
1000 genomes	rs104893981
hgdp	rs104893981
ensembl	rs104893981
geneview	rs104893981
scholar	rs104893981
google	rs104893981
pharmgkb	rs104893981
gwascentral	rs104893981
openSNP	rs104893981
23andMe	rs104893981
SNPshot	rs104893981
SNPdbe	rs104893981
MSV3d	rs104893981
GWAS Ctlg	rs104893981

Max Magnitude

0

OMIM	608272
Desc
Variant	0015
Related	also

ClinVar
Risk	rs104893981(T;T)
Alt	rs104893981(T;T)
Reference	Rs104893981(C;C)
Significance	Other
Disease	Sialidosis
Variation	info
Gene	NEU1
CLNDBN	Sialidosis, type II
Reversed	1
HGVS	NC_000006.11:g.31827947G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002561.4,