rs587780437

Orientation

minus

Stabilized

minus

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

Make rs587780437(A;A)

Make rs587780437(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

103523390

Gene

RELN

is a	snp
is	mentioned by
dbSNP	rs587780437
dbSNP (classic)	rs587780437
ClinGen	rs587780437
ebi	rs587780437
HLI	rs587780437
Exac	rs587780437
Gnomad	rs587780437
Varsome	rs587780437
LitVar	rs587780437
Map	rs587780437
PheGenI	rs587780437
Biobank	rs587780437
1000 genomes	rs587780437
hgdp	rs587780437
ensembl	rs587780437
geneview	rs587780437
scholar	rs587780437
google	rs587780437
pharmgkb	rs587780437
gwascentral	rs587780437
openSNP	rs587780437
23andMe	rs587780437
SNPshot	rs587780437
SNPdbe	rs587780437
MSV3d	rs587780437
GWAS Ctlg	rs587780437

Max Magnitude

0

ClinVar
Risk	rs587780437(A;A)
Alt	rs587780437(A;A)
Reference	Rs587780437(G;G)
Significance	Pathogenic
Disease	Lissencephaly 2 (Norman-Roberts type)
Variation	info
Gene	RELN
CLNDBN	Lissencephaly 2 (Norman-Roberts type)
Reversed	1
HGVS	NC_000007.13:g.103163837C>T
CLNSRC
CLNACC	RCV000118140.1,