rs362691

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs362691(C;C)

Make rs362691(C;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

103610714

Gene

RELN

is a	snp
is	mentioned by
dbSNP	rs362691
dbSNP (classic)	rs362691
ClinGen	rs362691
ebi	rs362691
HLI	rs362691
Exac	rs362691
Gnomad	rs362691
Varsome	rs362691
LitVar	rs362691
Map	rs362691
PheGenI	rs362691
Biobank	rs362691
1000 genomes	rs362691
hgdp	rs362691
ensembl	rs362691
geneview	rs362691
scholar	rs362691
google	rs362691
pharmgkb	rs362691
gwascentral	rs362691
openSNP	rs362691
23andMe	rs362691
SNPshot	rs362691
SNPdbe	rs362691
MSV3d	rs362691
GWAS Ctlg	rs362691

GMAF

0.1033

Max Magnitude

0

?

(C;C) (C;G) (G;G)

28

[PMID 20554015] No significant association between RELN polymorphism and autism in case-control and family-based association study in Chinese Han population [PMID 18597938] Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.

[PMID 20697953] An association analysis of reelin gene (RELN) polymorphisms with childhood epilepsy in eastern Indian population from West Bengal. [PMID 23216241 ] Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.

ClinVar
Risk	rs362691(A;A) rs362691(C;C)
Alt	rs362691(A;A) rs362691(C;C)
Reference	Rs362691(G;G)
Significance	Other
Disease	not specified Lissencephaly
Variation	info
Gene	RELN
CLNDBN	not specified Lissencephaly, Recessive
Reversed	0
HGVS	NC_000007.13:g.103251161G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000118147.4, RCV000330941.1,