rs863223388

Orientation

minus

Stabilized

minus

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

Make rs863223388(G;G)

Make rs863223388(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

103491969

Gene	LOC101927870, RELN

is a	snp
is	mentioned by
dbSNP	rs863223388
dbSNP (classic)	rs863223388
ClinGen	rs863223388
ebi	rs863223388
HLI	rs863223388
Exac	rs863223388
Gnomad	rs863223388
Varsome	rs863223388
LitVar	rs863223388
Map	rs863223388
PheGenI	rs863223388
Biobank	rs863223388
1000 genomes	rs863223388
hgdp	rs863223388
ensembl	rs863223388
geneview	rs863223388
scholar	rs863223388
google	rs863223388
pharmgkb	rs863223388
gwascentral	rs863223388
openSNP	rs863223388
23andMe	rs863223388
SNPshot	rs863223388
SNPdbe	rs863223388
MSV3d	rs863223388
GWAS Ctlg	rs863223388

Max Magnitude

0

ClinVar
Risk	rs863223388(G;G)
Alt	rs863223388(G;G)
Reference	Rs863223388(T;T)
Significance	Pathogenic
Disease	Abnormality of neuronal migration
Variation	info
Gene	LOC101927870 RELN
CLNDBN	Abnormality of neuronal migration
Reversed	1
HGVS	NC_000007.13:g.103132416A>C
CLNSRC
CLNACC	RCV000201320.1,