rs797044554

Orientation

plus

Stabilized

plus

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

Make rs797044554(-;AGCC)

Make rs797044554(AGCC;AGCC)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

53157430

Gene

DCC

is a	snp
is	mentioned by
dbSNP	rs797044554
dbSNP (classic)	rs797044554
ClinGen	rs797044554
ebi	rs797044554
HLI	rs797044554
Exac	rs797044554
Gnomad	rs797044554
Varsome	rs797044554
LitVar	rs797044554
Map	rs797044554
PheGenI	rs797044554
Biobank	rs797044554
1000 genomes	rs797044554
hgdp	rs797044554
ensembl	rs797044554
geneview	rs797044554
scholar	rs797044554
google	rs797044554
pharmgkb	rs797044554
gwascentral	rs797044554
openSNP	rs797044554
23andMe	rs797044554
SNPshot	rs797044554
SNPdbe	rs797044554
MSV3d	rs797044554
GWAS Ctlg	rs797044554

Max Magnitude

0

ClinVar
Risk	rs797044554(CCAG;CCAG)
Alt	rs797044554(CCAG;CCAG)
Reference	Rs797044554(-;-)
Significance	Pathogenic
Disease	Mirror movements 1
Variation	info
Gene	DCC
CLNDBN	Mirror movements 1
Reversed	0
HGVS	NC_000018.9:g.50683800_50683801insAGCC
CLNSRC
CLNACC	RCV000192081.1,