rs797044553

Orientation

plus

Stabilized

plus

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

Make rs797044553(A;A)

Make rs797044553(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

53063460

Gene

DCC

is a	snp
is	mentioned by
dbSNP	rs797044553
dbSNP (classic)	rs797044553
ClinGen	rs797044553
ebi	rs797044553
HLI	rs797044553
Exac	rs797044553
Gnomad	rs797044553
Varsome	rs797044553
LitVar	rs797044553
Map	rs797044553
PheGenI	rs797044553
Biobank	rs797044553
1000 genomes	rs797044553
hgdp	rs797044553
ensembl	rs797044553
geneview	rs797044553
scholar	rs797044553
google	rs797044553
pharmgkb	rs797044553
gwascentral	rs797044553
openSNP	rs797044553
23andMe	rs797044553
SNPshot	rs797044553
SNPdbe	rs797044553
MSV3d	rs797044553
GWAS Ctlg	rs797044553

Max Magnitude

0

ClinVar
Risk	rs797044553(A;A)
Alt	rs797044553(A;A)
Reference	Rs797044553(G;G)
Significance	Pathogenic
Disease	Mirror movements 1
Variation	info
Gene	DCC
CLNDBN	Mirror movements 1
Reversed	0
HGVS	NC_000018.9:g.50589830G>A
CLNSRC
CLNACC	RCV000192080.1,