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rs797044554

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044554(-;AGCC)
Make rs797044554(AGCC;AGCC)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position53157430
GeneDCC
is asnp
is mentioned by
dbSNPrs797044554
dbSNP (old)rs797044554
ClinGenrs797044554
ebirs797044554
HLIrs797044554
Exacrs797044554
Gnomadrs797044554
Varsomers797044554
Maprs797044554
PheGenIrs797044554
Biobankrs797044554
1000 genomesrs797044554
hgdprs797044554
ensemblrs797044554
gopubmedrs797044554
geneviewrs797044554
scholarrs797044554
googlers797044554
pharmgkbrs797044554
gwascentralrs797044554
openSNPrs797044554
23andMers797044554
23andMe allrs797044554
SNP Nexus

SNPshotrs797044554
SNPdbers797044554
MSV3drs797044554
GWAS Ctlgrs797044554
Max Magnitude0
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,