rs797044551

Orientation

plus

Stabilized

plus

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

Make rs797044551(A;A)

Make rs797044551(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

52752339

Gene

DCC

is a	snp
is	mentioned by
dbSNP	rs797044551
dbSNP (classic)	rs797044551
ClinGen	rs797044551
ebi	rs797044551
HLI	rs797044551
Exac	rs797044551
Gnomad	rs797044551
Varsome	rs797044551
LitVar	rs797044551
Map	rs797044551
PheGenI	rs797044551
Biobank	rs797044551
1000 genomes	rs797044551
hgdp	rs797044551
ensembl	rs797044551
geneview	rs797044551
scholar	rs797044551
google	rs797044551
pharmgkb	rs797044551
gwascentral	rs797044551
openSNP	rs797044551
23andMe	rs797044551
SNPshot	rs797044551
SNPdbe	rs797044551
MSV3d	rs797044551
GWAS Ctlg	rs797044551

Max Magnitude

0

ClinVar
Risk	rs797044551(A;A)
Alt	rs797044551(A;A)
Reference	Rs797044551(C;C)
Significance	Pathogenic
Disease	Mirror movements 1
Variation	info
Gene	DCC
CLNDBN	Mirror movements 1
Reversed	0
HGVS	NC_000018.9:g.50278709C>A
CLNSRC
CLNACC	RCV000192077.1,