rs863223389

Orientation

minus

Stabilized

minus

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

Make rs863223389(A;A)

Make rs863223389(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

103636325

Gene

RELN

is a	snp
is	mentioned by
dbSNP	rs863223389
dbSNP (classic)	rs863223389
ClinGen	rs863223389
ebi	rs863223389
HLI	rs863223389
Exac	rs863223389
Gnomad	rs863223389
Varsome	rs863223389
LitVar	rs863223389
Map	rs863223389
PheGenI	rs863223389
Biobank	rs863223389
1000 genomes	rs863223389
hgdp	rs863223389
ensembl	rs863223389
geneview	rs863223389
scholar	rs863223389
google	rs863223389
pharmgkb	rs863223389
gwascentral	rs863223389
openSNP	rs863223389
23andMe	rs863223389
SNPshot	rs863223389
SNPdbe	rs863223389
MSV3d	rs863223389
GWAS Ctlg	rs863223389

Max Magnitude

0

ClinVar
Risk	rs863223389(A;A)
Alt	rs863223389(A;A)
Reference	Rs863223389(G;G)
Significance	Pathogenic
Disease	Abnormality of neuronal migration
Variation	info
Gene	RELN
CLNDBN	Abnormality of neuronal migration
Reversed	1
HGVS	NC_000007.13:g.103276772C>T
CLNSRC
CLNACC	RCV000201320.1,