rs1057518119

Orientation

plus

Stabilized

plus

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

Make rs1057518119(A;A)

Make rs1057518119(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

129314799

Gene

LAMA2

is a	snp
is	mentioned by
dbSNP	rs1057518119
dbSNP (classic)	rs1057518119
ClinGen	rs1057518119
ebi	rs1057518119
HLI	rs1057518119
Exac	rs1057518119
Gnomad	rs1057518119
Varsome	rs1057518119
LitVar	rs1057518119
Map	rs1057518119
PheGenI	rs1057518119
Biobank	rs1057518119
1000 genomes	rs1057518119
hgdp	rs1057518119
ensembl	rs1057518119
geneview	rs1057518119
scholar	rs1057518119
google	rs1057518119
pharmgkb	rs1057518119
gwascentral	rs1057518119
openSNP	rs1057518119
23andMe	rs1057518119
SNPshot	rs1057518119
SNPdbe	rs1057518119
MSV3d	rs1057518119
GWAS Ctlg	rs1057518119

Max Magnitude

0

ClinVar
Risk	rs1057518119(A;A)
Alt	rs1057518119(A;A)
Reference	Rs1057518119(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LAMA2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.129635944G>A
CLNSRC
CLNACC	RCV000413320.1,