Have questions? Visit https://www.reddit.com/r/SNPedia

rs797044552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044552(-;G)
Make rs797044552(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position52906202
GeneDCC
is asnp
is mentioned by
dbSNPrs797044552
ClinGenrs797044552
ebirs797044552
HLIrs797044552
Exacrs797044552
Varsomers797044552
Maprs797044552
PheGenIrs797044552
hapmaprs797044552
1000 genomesrs797044552
hgdprs797044552
ensemblrs797044552
gopubmedrs797044552
geneviewrs797044552
scholarrs797044552
googlers797044552
pharmgkbrs797044552
gwascentralrs797044552
openSNPrs797044552
23andMers797044552
23andMe allrs797044552
SNP Nexus

SNPshotrs797044552
SNPdbers797044552
MSV3drs797044552
GWAS Ctlgrs797044552
Max Magnitude0
ClinVar
Risk rs797044552(G;G)
Alt rs797044552(G;G)
Reference Rs797044552(-;-)
Significance Pathogenic
Disease Mirror movements 1
Variation info
Gene DCC
CLNDBN Mirror movements 1
Reversed 0
HGVS NC_000018.9:g.50432572dupG
CLNSRC
CLNACC RCV000192078.1,