rs112039851

Orientation

plus

Stabilized

plus

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

Make rs112039851(C;C)

Make rs112039851(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

1045444

Gene

AGRN

is a	snp
is	mentioned by
dbSNP	rs112039851
dbSNP (classic)	rs112039851
ClinGen	rs112039851
ebi	rs112039851
HLI	rs112039851
Exac	rs112039851
Gnomad	rs112039851
Varsome	rs112039851
LitVar	rs112039851
Map	rs112039851
PheGenI	rs112039851
Biobank	rs112039851
1000 genomes	rs112039851
hgdp	rs112039851
ensembl	rs112039851
geneview	rs112039851
scholar	rs112039851
google	rs112039851
pharmgkb	rs112039851
gwascentral	rs112039851
openSNP	rs112039851
23andMe	rs112039851
SNPshot	rs112039851
SNPdbe	rs112039851
MSV3d	rs112039851
GWAS Ctlg	rs112039851

Max Magnitude

0

ClinVar
Risk	rs112039851(A;A) rs112039851(C;C)
Alt	rs112039851(A;A) rs112039851(C;C)
Reference	Rs112039851(G;G)
Significance	Other
Disease	not specified
Variation	info
Gene	AGRN
CLNDBN	not specified
Reversed	0
HGVS	NC_000001.10:g.980824G>C
CLNSRC
CLNACC	RCV000246474.2,