rs869320767

Orientation

minus

Stabilized

minus

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

Make rs869320767(A;A)

Make rs869320767(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

103553659

Gene

RELN

is a	snp
is	mentioned by
dbSNP	rs869320767
dbSNP (classic)	rs869320767
ClinGen	rs869320767
ebi	rs869320767
HLI	rs869320767
Exac	rs869320767
Gnomad	rs869320767
Varsome	rs869320767
LitVar	rs869320767
Map	rs869320767
PheGenI	rs869320767
Biobank	rs869320767
1000 genomes	rs869320767
hgdp	rs869320767
ensembl	rs869320767
geneview	rs869320767
scholar	rs869320767
google	rs869320767
pharmgkb	rs869320767
gwascentral	rs869320767
openSNP	rs869320767
23andMe	rs869320767
SNPshot	rs869320767
SNPdbe	rs869320767
MSV3d	rs869320767
GWAS Ctlg	rs869320767

Max Magnitude

0

ClinVar
Risk	rs869320767(A;A)
Alt	rs869320767(A;A)
Reference	Rs869320767(G;G)
Significance	Pathogenic
Disease	Lissencephaly 2
Variation	info
Gene	RELN
CLNDBN	Lissencephaly 2
Reversed	1
HGVS	NC_000007.13:g.103194106C>T
CLNSRC
CLNACC	RCV000210930.1,