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rs754914260

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs754914260(A;A)
Make rs754914260(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position52923832
GeneDCC
is asnp
is mentioned by
dbSNPrs754914260
ebirs754914260
HLIrs754914260
Exacrs754914260
Varsomers754914260
Maprs754914260
PheGenIrs754914260
hapmaprs754914260
1000 genomesrs754914260
hgdprs754914260
ensemblrs754914260
gopubmedrs754914260
geneviewrs754914260
scholarrs754914260
googlers754914260
pharmgkbrs754914260
gwascentralrs754914260
openSNPrs754914260
23andMers754914260
23andMe allrs754914260
SNP Nexus

SNPshotrs754914260
SNPdbers754914260
MSV3drs754914260
GWAS Ctlgrs754914260
Max Magnitude0
ClinVar
Risk rs754914260(A;A)
Alt rs754914260(A;A)
Reference rs754914260(C;C)
Significance Pathogenic
Disease Mirror movements
Variation info
Gene DCC
CLNDBN Mirror movements, congenital
Reversed 0
HGVS NC_000018.9:g.50450202C>T
CLNSRC
CLNACC RCV000192079.1,