rs1057517963

Orientation

plus

Stabilized

plus

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

Make rs1057517963(A;G)

Make rs1057517963(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

129502657

Gene	LAMA2, LOC102723409

is a	snp
is	mentioned by
dbSNP	rs1057517963
dbSNP (classic)	rs1057517963
ClinGen	rs1057517963
ebi	rs1057517963
HLI	rs1057517963
Exac	rs1057517963
Gnomad	rs1057517963
Varsome	rs1057517963
LitVar	rs1057517963
Map	rs1057517963
PheGenI	rs1057517963
Biobank	rs1057517963
1000 genomes	rs1057517963
hgdp	rs1057517963
ensembl	rs1057517963
geneview	rs1057517963
scholar	rs1057517963
google	rs1057517963
pharmgkb	rs1057517963
gwascentral	rs1057517963
openSNP	rs1057517963
23andMe	rs1057517963
SNPshot	rs1057517963
SNPdbe	rs1057517963
MSV3d	rs1057517963
GWAS Ctlg	rs1057517963

Max Magnitude

0

ClinVar
Risk	rs1057517963(G;G)
Alt	rs1057517963(G;G)
Reference	Rs1057517963(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LAMA2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.129823802A>G
CLNSRC
CLNACC	RCV000414051.1,