rs1057517756

Orientation

minus

Stabilized

minus

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

Make rs1057517756(C;T)

Make rs1057517756(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

7049182

Gene

LAMA1

is a	snp
is	mentioned by
dbSNP	rs1057517756
dbSNP (classic)	rs1057517756
ClinGen	rs1057517756
ebi	rs1057517756
HLI	rs1057517756
Exac	rs1057517756
Gnomad	rs1057517756
Varsome	rs1057517756
LitVar	rs1057517756
Map	rs1057517756
PheGenI	rs1057517756
Biobank	rs1057517756
1000 genomes	rs1057517756
hgdp	rs1057517756
ensembl	rs1057517756
geneview	rs1057517756
scholar	rs1057517756
google	rs1057517756
pharmgkb	rs1057517756
gwascentral	rs1057517756
openSNP	rs1057517756
23andMe	rs1057517756
SNPshot	rs1057517756
SNPdbe	rs1057517756
MSV3d	rs1057517756
GWAS Ctlg	rs1057517756

Max Magnitude

0

ClinVar
Risk	rs1057517756(T;T)
Alt	rs1057517756(T;T)
Reference	Rs1057517756(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LAMA1
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.7049181G>A
CLNSRC
CLNACC	RCV000414527.1,