rs754323928

Orientation

plus

Stabilized

plus

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

Make rs754323928(C;G)

Make rs754323928(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

23876394

Gene

LAMA3

is a	snp
is	mentioned by
dbSNP	rs754323928
dbSNP (classic)	rs754323928
ClinGen	rs754323928
ebi	rs754323928
HLI	rs754323928
Exac	rs754323928
Gnomad	rs754323928
Varsome	rs754323928
LitVar	rs754323928
Map	rs754323928
PheGenI	rs754323928
Biobank	rs754323928
1000 genomes	rs754323928
hgdp	rs754323928
ensembl	rs754323928
geneview	rs754323928
scholar	rs754323928
google	rs754323928
pharmgkb	rs754323928
gwascentral	rs754323928
openSNP	rs754323928
23andMe	rs754323928
SNPshot	rs754323928
SNPdbe	rs754323928
MSV3d	rs754323928
GWAS Ctlg	rs754323928

Max Magnitude

0

ClinVar
Risk	rs754323928(G;G)
Alt	rs754323928(G;G)
Reference	Rs754323928(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LAMA3
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.21456358C>G
CLNSRC
CLNACC	RCV000484655.1,