rs786205657

Orientation

minus

Stabilized

minus

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

Make rs786205657(-;-)

Make rs786205657(-;AT)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

103539227

Gene	LOC105375435, RELN

is a	snp
is	mentioned by
dbSNP	rs786205657
dbSNP (classic)	rs786205657
ClinGen	rs786205657
ebi	rs786205657
HLI	rs786205657
Exac	rs786205657
Gnomad	rs786205657
Varsome	rs786205657
LitVar	rs786205657
Map	rs786205657
PheGenI	rs786205657
Biobank	rs786205657
1000 genomes	rs786205657
hgdp	rs786205657
ensembl	rs786205657
geneview	rs786205657
scholar	rs786205657
google	rs786205657
pharmgkb	rs786205657
gwascentral	rs786205657
openSNP	rs786205657
23andMe	rs786205657
SNPshot	rs786205657
SNPdbe	rs786205657
MSV3d	rs786205657
GWAS Ctlg	rs786205657

Max Magnitude

0

ClinVar
Risk	rs786205657(-;-)
Alt	rs786205657(-;-)
Reference	Rs786205657(AT;AT)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RELN
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.103179674_103179675delAT
CLNSRC
CLNACC	RCV000171531.1,