rs200923373

Orientation

plus

Stabilized

plus

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

Make rs200923373(C;T)

Make rs200923373(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

129342379

Gene

LAMA2

is a	snp
is	mentioned by
dbSNP	rs200923373
dbSNP (classic)	rs200923373
ClinGen	rs200923373
ebi	rs200923373
HLI	rs200923373
Exac	rs200923373
Gnomad	rs200923373
Varsome	rs200923373
LitVar	rs200923373
Map	rs200923373
PheGenI	rs200923373
Biobank	rs200923373
1000 genomes	rs200923373
hgdp	rs200923373
ensembl	rs200923373
geneview	rs200923373
scholar	rs200923373
google	rs200923373
pharmgkb	rs200923373
gwascentral	rs200923373
openSNP	rs200923373
23andMe	rs200923373
SNPshot	rs200923373
SNPdbe	rs200923373
MSV3d	rs200923373
GWAS Ctlg	rs200923373

Max Magnitude

0

ClinVar
Risk	rs200923373(T;T)
Alt	rs200923373(T;T)
Reference	Rs200923373(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LAMA2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.129663524C>T
CLNSRC
CLNACC	RCV000171401.1,