rs797044552

Orientation

plus

Stabilized

plus

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

Make rs797044552(-;G)

Make rs797044552(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

52906202

Gene

DCC

is a	snp
is	mentioned by
dbSNP	rs797044552
dbSNP (classic)	rs797044552
ClinGen	rs797044552
ebi	rs797044552
HLI	rs797044552
Exac	rs797044552
Gnomad	rs797044552
Varsome	rs797044552
LitVar	rs797044552
Map	rs797044552
PheGenI	rs797044552
Biobank	rs797044552
1000 genomes	rs797044552
hgdp	rs797044552
ensembl	rs797044552
geneview	rs797044552
scholar	rs797044552
google	rs797044552
pharmgkb	rs797044552
gwascentral	rs797044552
openSNP	rs797044552
23andMe	rs797044552
SNPshot	rs797044552
SNPdbe	rs797044552
MSV3d	rs797044552
GWAS Ctlg	rs797044552

Max Magnitude

0

ClinVar
Risk	rs797044552(G;G)
Alt	rs797044552(G;G)
Reference	Rs797044552(-;-)
Significance	Pathogenic
Disease	Mirror movements 1
Variation	info
Gene	DCC
CLNDBN	Mirror movements 1
Reversed	0
HGVS	NC_000018.9:g.50432572dupG
CLNSRC
CLNACC	RCV000192078.1,