rs398123455

Orientation

minus

Stabilized

minus

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

Make rs398123455(A;A)

Make rs398123455(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

12652270

Gene

MAN2B1

is a	snp
is	mentioned by
dbSNP	rs398123455
dbSNP (classic)	rs398123455
ClinGen	rs398123455
ebi	rs398123455
HLI	rs398123455
Exac	rs398123455
Gnomad	rs398123455
Varsome	rs398123455
LitVar	rs398123455
Map	rs398123455
PheGenI	rs398123455
Biobank	rs398123455
1000 genomes	rs398123455
hgdp	rs398123455
ensembl	rs398123455
geneview	rs398123455
scholar	rs398123455
google	rs398123455
pharmgkb	rs398123455
gwascentral	rs398123455
openSNP	rs398123455
23andMe	rs398123455
SNPshot	rs398123455
SNPdbe	rs398123455
MSV3d	rs398123455
GWAS Ctlg	rs398123455

Max Magnitude

0

ClinVar
Risk	rs398123455(A;A)
Alt	rs398123455(A;A)
Reference	Rs398123455(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MAN2B1
CLNDBN	not provided
Reversed	1
HGVS	NC_000019.9:g.12763084C>T
CLNSRC	HGMD
CLNACC	RCV000079075.4,