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rs797044553

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044553(A;A)
Make rs797044553(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position53063460
GeneDCC
is asnp
is mentioned by
dbSNPrs797044553
ebirs797044553
HLIrs797044553
Exacrs797044553
Varsomers797044553
Maprs797044553
PheGenIrs797044553
hapmaprs797044553
1000 genomesrs797044553
hgdprs797044553
ensemblrs797044553
gopubmedrs797044553
geneviewrs797044553
scholarrs797044553
googlers797044553
pharmgkbrs797044553
gwascentralrs797044553
openSNPrs797044553
23andMers797044553
23andMe allrs797044553
SNP Nexus

SNPshotrs797044553
SNPdbers797044553
MSV3drs797044553
GWAS Ctlgrs797044553
Max Magnitude0
ClinVar
Risk rs797044553(A;A)
Alt rs797044553(A;A)
Reference rs797044553(G;G)
Significance Pathogenic
Disease Mirror movements
Variation info
Gene DCC
CLNDBN Mirror movements, congenital
Reversed 0
HGVS NC_000018.9:g.50589830G>A
CLNSRC
CLNACC RCV000192080.1,