rs607755

Orientation

plus

Stabilized

plus

Make rs607755(A;A)

Make rs607755(A;G)

Make rs607755(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

103749507

Gene

RELN

is a	snp
is	mentioned by
dbSNP	rs607755
dbSNP (classic)	rs607755
ClinGen	rs607755
ebi	rs607755
HLI	rs607755
Exac	rs607755
Gnomad	rs607755
Varsome	rs607755
LitVar	rs607755
Map	rs607755
PheGenI	rs607755
Biobank	rs607755
1000 genomes	rs607755
hgdp	rs607755
ensembl	rs607755
geneview	rs607755
scholar	rs607755
google	rs607755
pharmgkb	rs607755
gwascentral	rs607755
openSNP	rs607755
23andMe	rs607755
SNPshot	rs607755
SNPdbe	rs607755
MSV3d	rs607755
GWAS Ctlg	rs607755

GMAF

0.4651

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 18599960] rs607755 and rs2229874 appear to relate to females and Alzheimer's disease

ClinVar
Risk	rs607755(G;G)
Alt	rs607755(G;G)
Reference	rs607755(A;A)
Significance	Other
Disease	not specified Lissencephaly
Variation	info
Gene	RELN
CLNDBN	not specified Lissencephaly, Recessive
Reversed	0
HGVS	NC_000007.13:g.103389954A>G
CLNSRC	ClinVar University of Chicago
CLNACC	RCV000081236.8, RCV000402466.1,