rs886039412

Orientation

plus

Stabilized

plus

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

Make rs886039412(A;A)

Make rs886039412(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

18

Position

23928766

Gene

LAMA3

is a	snp
is	mentioned by
dbSNP	rs886039412
dbSNP (classic)	rs886039412
ClinGen	rs886039412
ebi	rs886039412
HLI	rs886039412
Exac	rs886039412
Gnomad	rs886039412
Varsome	rs886039412
LitVar	rs886039412
Map	rs886039412
PheGenI	rs886039412
Biobank	rs886039412
1000 genomes	rs886039412
hgdp	rs886039412
ensembl	rs886039412
geneview	rs886039412
scholar	rs886039412
google	rs886039412
pharmgkb	rs886039412
gwascentral	rs886039412
openSNP	rs886039412
23andMe	rs886039412
SNPshot	rs886039412
SNPdbe	rs886039412
MSV3d	rs886039412
GWAS Ctlg	rs886039412

Max Magnitude

0

ClinVar
Risk	rs886039412(A;A)
Alt	rs886039412(A;A)
Reference	Rs886039412(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LAMA3
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.21508730G>A
CLNSRC
CLNACC	RCV000255139.1,