rs1064797328

Orientation

plus

Stabilized

plus

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

Chromosome

6

Position

129460317

Gene

LAMA2

is a	snp
is	mentioned by
dbSNP	rs1064797328
dbSNP (classic)	rs1064797328
ClinGen	rs1064797328
ebi	rs1064797328
HLI	rs1064797328
Exac	rs1064797328
Gnomad	rs1064797328
Varsome	rs1064797328
LitVar	rs1064797328
Map	rs1064797328
PheGenI	rs1064797328
Biobank	rs1064797328
1000 genomes	rs1064797328
hgdp	rs1064797328
ensembl	rs1064797328
geneview	rs1064797328
scholar	rs1064797328
google	rs1064797328
pharmgkb	rs1064797328
gwascentral	rs1064797328
openSNP	rs1064797328
23andMe	rs1064797328
SNPshot	rs1064797328
SNPdbe	rs1064797328
MSV3d	rs1064797328
GWAS Ctlg	rs1064797328

Max Magnitude

0

ClinVar
Risk	rs1064797328(-;-)
Alt	rs1064797328(-;-)
Reference	Rs1064797328(ACTG;ACTG)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LAMA2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.129781462_129781465delACTG
CLNSRC
CLNACC	RCV000488369.1,