rs1057524616

Orientation

plus

Stabilized

plus

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

Make rs1057524616(G;T)

Make rs1057524616(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

129342472

Gene

LAMA2

is a	snp
is	mentioned by
dbSNP	rs1057524616
dbSNP (classic)	rs1057524616
ClinGen	rs1057524616
ebi	rs1057524616
HLI	rs1057524616
Exac	rs1057524616
Gnomad	rs1057524616
Varsome	rs1057524616
LitVar	rs1057524616
Map	rs1057524616
PheGenI	rs1057524616
Biobank	rs1057524616
1000 genomes	rs1057524616
hgdp	rs1057524616
ensembl	rs1057524616
geneview	rs1057524616
scholar	rs1057524616
google	rs1057524616
pharmgkb	rs1057524616
gwascentral	rs1057524616
openSNP	rs1057524616
23andMe	rs1057524616
SNPshot	rs1057524616
SNPdbe	rs1057524616
MSV3d	rs1057524616
GWAS Ctlg	rs1057524616

Max Magnitude

0

ClinVar
Risk	rs1057524616(T;T)
Alt	rs1057524616(T;T)
Reference	Rs1057524616(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LAMA2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.129663617G>T
CLNSRC
CLNACC	RCV000424965.1,