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rs797044551

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044551(A;A)
Make rs797044551(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position52752339
GeneDCC
is asnp
is mentioned by
dbSNPrs797044551
ebirs797044551
HLIrs797044551
Exacrs797044551
Varsomers797044551
Maprs797044551
PheGenIrs797044551
hapmaprs797044551
1000 genomesrs797044551
hgdprs797044551
ensemblrs797044551
gopubmedrs797044551
geneviewrs797044551
scholarrs797044551
googlers797044551
pharmgkbrs797044551
gwascentralrs797044551
openSNPrs797044551
23andMers797044551
23andMe allrs797044551
SNP Nexus

SNPshotrs797044551
SNPdbers797044551
MSV3drs797044551
GWAS Ctlgrs797044551
Max Magnitude0
ClinVar
Risk rs797044551(A;A)
Alt rs797044551(A;A)
Reference rs797044551(C;C)
Significance Pathogenic
Disease Mirror movements
Variation info
Gene DCC
CLNDBN Mirror movements, congenital
Reversed 0
HGVS NC_000018.9:g.50278709C>A
CLNSRC
CLNACC RCV000192077.1,