rs773209126

Orientation

plus

Stabilized

plus

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

Make rs773209126(C;T)

Make rs773209126(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

6

Position

129165672

Gene

LAMA2

is a	snp
is	mentioned by
dbSNP	rs773209126
dbSNP (classic)	rs773209126
ClinGen	rs773209126
ebi	rs773209126
HLI	rs773209126
Exac	rs773209126
Gnomad	rs773209126
Varsome	rs773209126
LitVar	rs773209126
Map	rs773209126
PheGenI	rs773209126
Biobank	rs773209126
1000 genomes	rs773209126
hgdp	rs773209126
ensembl	rs773209126
geneview	rs773209126
scholar	rs773209126
google	rs773209126
pharmgkb	rs773209126
gwascentral	rs773209126
openSNP	rs773209126
23andMe	rs773209126
SNPshot	rs773209126
SNPdbe	rs773209126
MSV3d	rs773209126
GWAS Ctlg	rs773209126

Max Magnitude

0

ClinVar
Risk	rs773209126(T;T)
Alt	rs773209126(T;T)
Reference	Rs773209126(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LAMA2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.129486817C>T
CLNSRC
CLNACC	RCV000224579.1,