rs587780435

Orientation

minus

Stabilized

minus

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

Make rs587780435(A;A)

Make rs587780435(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

103565295

Gene

RELN

is a	snp
is	mentioned by
dbSNP	rs587780435
dbSNP (classic)	rs587780435
ClinGen	rs587780435
ebi	rs587780435
HLI	rs587780435
Exac	rs587780435
Gnomad	rs587780435
Varsome	rs587780435
LitVar	rs587780435
Map	rs587780435
PheGenI	rs587780435
Biobank	rs587780435
1000 genomes	rs587780435
hgdp	rs587780435
ensembl	rs587780435
geneview	rs587780435
scholar	rs587780435
google	rs587780435
pharmgkb	rs587780435
gwascentral	rs587780435
openSNP	rs587780435
23andMe	rs587780435
SNPshot	rs587780435
SNPdbe	rs587780435
MSV3d	rs587780435
GWAS Ctlg	rs587780435

Max Magnitude

0

ClinVar
Risk	rs587780435(A;A)
Alt	rs587780435(A;A)
Reference	Rs587780435(C;C)
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.103205742G>T
CLNSRC
CLNACC	RCV000118138.1,