rs770458492

Orientation

plus

Stabilized

plus

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

Make rs770458492(C;G)

Make rs770458492(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

8806370

Gene

PMM2

is a	snp
is	mentioned by
dbSNP	rs770458492
dbSNP (classic)	rs770458492
ClinGen	rs770458492
ebi	rs770458492
HLI	rs770458492
Exac	rs770458492
Gnomad	rs770458492
Varsome	rs770458492
LitVar	rs770458492
Map	rs770458492
PheGenI	rs770458492
Biobank	rs770458492
1000 genomes	rs770458492
hgdp	rs770458492
ensembl	rs770458492
geneview	rs770458492
scholar	rs770458492
google	rs770458492
pharmgkb	rs770458492
gwascentral	rs770458492
openSNP	rs770458492
23andMe	rs770458492
SNPshot	rs770458492
SNPdbe	rs770458492
MSV3d	rs770458492
GWAS Ctlg	rs770458492

Max Magnitude

0

ClinVar
Risk	rs770458492(G;G)
Alt	rs770458492(G;G)
Reference	Rs770458492(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PMM2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.8900227C>G
CLNSRC
CLNACC	RCV000437277.1,