rs797045912

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(D;D)	0	common genotype

Make rs797045912(-;T)

Make rs797045912(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

103917082

Gene

RELN

is a	snp
is	mentioned by
dbSNP	rs797045912
dbSNP (classic)	rs797045912
ClinGen	rs797045912
ebi	rs797045912
HLI	rs797045912
Exac	rs797045912
Gnomad	rs797045912
Varsome	rs797045912
LitVar	rs797045912
Map	rs797045912
PheGenI	rs797045912
Biobank	rs797045912
1000 genomes	rs797045912
hgdp	rs797045912
ensembl	rs797045912
geneview	rs797045912
scholar	rs797045912
google	rs797045912
pharmgkb	rs797045912
gwascentral	rs797045912
openSNP	rs797045912
23andMe	rs797045912
SNPshot	rs797045912
SNPdbe	rs797045912
MSV3d	rs797045912
GWAS Ctlg	rs797045912

Max Magnitude

0

ClinVar
Risk	rs797045912(T;T)
Alt	rs797045912(T;T)
Reference	Rs797045912(-;-)
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.103557530dupA
CLNSRC
CLNACC	RCV000192487.1,