rs765943112

Orientation

plus

Stabilized

plus

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

Make rs765943112(G;G)

Make rs765943112(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

23864885

Gene

LAMA3

is a	snp
is	mentioned by
dbSNP	rs765943112
dbSNP (classic)	rs765943112
ClinGen	rs765943112
ebi	rs765943112
HLI	rs765943112
Exac	rs765943112
Gnomad	rs765943112
Varsome	rs765943112
LitVar	rs765943112
Map	rs765943112
PheGenI	rs765943112
Biobank	rs765943112
1000 genomes	rs765943112
hgdp	rs765943112
ensembl	rs765943112
geneview	rs765943112
scholar	rs765943112
google	rs765943112
pharmgkb	rs765943112
gwascentral	rs765943112
openSNP	rs765943112
23andMe	rs765943112
SNPshot	rs765943112
SNPdbe	rs765943112
MSV3d	rs765943112
GWAS Ctlg	rs765943112

Max Magnitude

0

ClinVar
Risk	rs765943112(G;G)
Alt	rs765943112(G;G)
Reference	Rs765943112(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LAMA3
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.21444849T>G
CLNSRC
CLNACC	RCV000443726.1,