rs786205643

Orientation

minus

Stabilized

minus

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

Make rs786205643(A;C)

Make rs786205643(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

49132281

Gene

LAMB2

is a	snp
is	mentioned by
dbSNP	rs786205643
dbSNP (classic)	rs786205643
ClinGen	rs786205643
ebi	rs786205643
HLI	rs786205643
Exac	rs786205643
Gnomad	rs786205643
Varsome	rs786205643
LitVar	rs786205643
Map	rs786205643
PheGenI	rs786205643
Biobank	rs786205643
1000 genomes	rs786205643
hgdp	rs786205643
ensembl	rs786205643
geneview	rs786205643
scholar	rs786205643
google	rs786205643
pharmgkb	rs786205643
gwascentral	rs786205643
openSNP	rs786205643
23andMe	rs786205643
SNPshot	rs786205643
SNPdbe	rs786205643
MSV3d	rs786205643
GWAS Ctlg	rs786205643

Max Magnitude

0

ClinVar
Risk	rs786205643(C;C)
Alt	rs786205643(C;C)
Reference	Rs786205643(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LAMB2
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.49169714T>G
CLNSRC
CLNACC	RCV000171513.1,