rs117422805

Orientation

plus

Stabilized

plus

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

Make rs117422805(C;T)

Make rs117422805(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

129280072

Gene

LAMA2

is a	snp
is	mentioned by
dbSNP	rs117422805
dbSNP (classic)	rs117422805
ClinGen	rs117422805
ebi	rs117422805
HLI	rs117422805
Exac	rs117422805
Gnomad	rs117422805
Varsome	rs117422805
LitVar	rs117422805
Map	rs117422805
PheGenI	rs117422805
Biobank	rs117422805
1000 genomes	rs117422805
hgdp	rs117422805
ensembl	rs117422805
geneview	rs117422805
scholar	rs117422805
google	rs117422805
pharmgkb	rs117422805
gwascentral	rs117422805
openSNP	rs117422805
23andMe	rs117422805
SNPshot	rs117422805
SNPdbe	rs117422805
MSV3d	rs117422805
GWAS Ctlg	rs117422805

Max Magnitude

0

ClinVar
Risk	rs117422805(T;T)
Alt	rs117422805(T;T)
Reference	Rs117422805(C;C)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	LAMA2
CLNDBN	not specified
Reversed	0
HGVS	NC_000006.11:g.129601217C>T
CLNSRC
CLNACC	RCV000149994.3,