rs797044555

Orientation

plus

Stabilized

plus

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

Make rs797044555(-;AGGGA)

Make rs797044555(AGGGA;AGGGA)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

53402833

Gene

DCC

is a	snp
is	mentioned by
dbSNP	rs797044555
dbSNP (classic)	rs797044555
ClinGen	rs797044555
ebi	rs797044555
HLI	rs797044555
Exac	rs797044555
Gnomad	rs797044555
Varsome	rs797044555
LitVar	rs797044555
Map	rs797044555
PheGenI	rs797044555
Biobank	rs797044555
1000 genomes	rs797044555
hgdp	rs797044555
ensembl	rs797044555
geneview	rs797044555
scholar	rs797044555
google	rs797044555
pharmgkb	rs797044555
gwascentral	rs797044555
openSNP	rs797044555
23andMe	rs797044555
SNPshot	rs797044555
SNPdbe	rs797044555
MSV3d	rs797044555
GWAS Ctlg	rs797044555

Max Magnitude

0

ClinVar
Risk	rs797044555(AGGGA;AGGGA)
Alt	rs797044555(AGGGA;AGGGA)
Reference	Rs797044555(-;-)
Significance	Pathogenic
Disease	Mirror movements 1
Variation	info
Gene	DCC
CLNDBN	Mirror movements 1
Reversed	0
HGVS	NC_000018.9:g.50929199_50929203dupAGGGA
CLNSRC
CLNACC	RCV000192082.1,