rs879255267

Orientation

minus

Stabilized

minus

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

Make rs879255267(G;T)

Make rs879255267(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

107975026

Gene

LAMB1

is a	snp
is	mentioned by
dbSNP	rs879255267
dbSNP (classic)	rs879255267
ClinGen	rs879255267
ebi	rs879255267
HLI	rs879255267
Exac	rs879255267
Gnomad	rs879255267
Varsome	rs879255267
LitVar	rs879255267
Map	rs879255267
PheGenI	rs879255267
Biobank	rs879255267
1000 genomes	rs879255267
hgdp	rs879255267
ensembl	rs879255267
geneview	rs879255267
scholar	rs879255267
google	rs879255267
pharmgkb	rs879255267
gwascentral	rs879255267
openSNP	rs879255267
23andMe	rs879255267
SNPshot	rs879255267
SNPdbe	rs879255267
MSV3d	rs879255267
GWAS Ctlg	rs879255267

Max Magnitude

0

ClinVar
Risk	rs879255267(T;T)
Alt	rs879255267(T;T)
Reference	Rs879255267(G;G)
Significance	Pathogenic
Disease	Lissencephaly 5
Variation	info
Gene	LAMB1
CLNDBN	Lissencephaly 5
Reversed	1
HGVS	NC_000007.13:g.107615471C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000210961.1,