rs797045915

Orientation

minus

Stabilized

minus

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

Make rs797045915(C;T)

Make rs797045915(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

103557992

Gene

RELN

is a	snp
is	mentioned by
dbSNP	rs797045915
dbSNP (classic)	rs797045915
ClinGen	rs797045915
ebi	rs797045915
HLI	rs797045915
Exac	rs797045915
Gnomad	rs797045915
Varsome	rs797045915
LitVar	rs797045915
Map	rs797045915
PheGenI	rs797045915
Biobank	rs797045915
1000 genomes	rs797045915
hgdp	rs797045915
ensembl	rs797045915
geneview	rs797045915
scholar	rs797045915
google	rs797045915
pharmgkb	rs797045915
gwascentral	rs797045915
openSNP	rs797045915
23andMe	rs797045915
SNPshot	rs797045915
SNPdbe	rs797045915
MSV3d	rs797045915
GWAS Ctlg	rs797045915

Max Magnitude

0

ClinVar
Risk	rs797045915(T;T)
Alt	rs797045915(T;T)
Reference	Rs797045915(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.103198439G>A
CLNSRC
CLNACC	RCV000194711.1,