rs797044556

Orientation

plus

Stabilized

plus

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

Make rs797044556(-;-)

Make rs797044556(-;CT)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

53486895

Gene

DCC

is a	snp
is	mentioned by
dbSNP	rs797044556
dbSNP (classic)	rs797044556
ClinGen	rs797044556
ebi	rs797044556
HLI	rs797044556
Exac	rs797044556
Gnomad	rs797044556
Varsome	rs797044556
LitVar	rs797044556
Map	rs797044556
PheGenI	rs797044556
Biobank	rs797044556
1000 genomes	rs797044556
hgdp	rs797044556
ensembl	rs797044556
geneview	rs797044556
scholar	rs797044556
google	rs797044556
pharmgkb	rs797044556
gwascentral	rs797044556
openSNP	rs797044556
23andMe	rs797044556
SNPshot	rs797044556
SNPdbe	rs797044556
MSV3d	rs797044556
GWAS Ctlg	rs797044556

Max Magnitude

0

ClinVar
Risk	rs797044556(-;-)
Alt	rs797044556(-;-)
Reference	Rs797044556(CT;CT)
Significance	Pathogenic
Disease	Mirror movements 1
Variation	info
Gene	DCC
CLNDBN	Mirror movements 1
Reversed	0
HGVS	NC_000018.9:g.51013265_51013266delCT
CLNSRC
CLNACC	RCV000192083.1,