rs398123392

Orientation

minus

Stabilized

minus

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

Make rs398123392(A;C)

Make rs398123392(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

31861259

Gene

NEU1

is a	snp
is	mentioned by
dbSNP	rs398123392
dbSNP (classic)	rs398123392
ClinGen	rs398123392
ebi	rs398123392
HLI	rs398123392
Exac	rs398123392
Gnomad	rs398123392
Varsome	rs398123392
LitVar	rs398123392
Map	rs398123392
PheGenI	rs398123392
Biobank	rs398123392
1000 genomes	rs398123392
hgdp	rs398123392
ensembl	rs398123392
geneview	rs398123392
scholar	rs398123392
google	rs398123392
pharmgkb	rs398123392
gwascentral	rs398123392
openSNP	rs398123392
23andMe	rs398123392
SNPshot	rs398123392
SNPdbe	rs398123392
MSV3d	rs398123392
GWAS Ctlg	rs398123392

Max Magnitude

0

ClinVar
Risk	rs398123392(C;C) rs398123392(G;G)
Alt	rs398123392(C;C) rs398123392(G;G)
Reference	Rs398123392(A;A)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	NEU1
CLNDBN	not provided not specified
Reversed	1
HGVS	NC_000006.11:g.31829036T>C; NC_000006.11:g.31829036T>G
CLNSRC
CLNACC	RCV000492831.1, RCV000078815.4,