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rs797044555

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044555(-;AGGGA)
Make rs797044555(AGGGA;AGGGA)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position53402833
GeneDCC
is asnp
is mentioned by
dbSNPrs797044555
ClinGenrs797044555
ebirs797044555
HLIrs797044555
Exacrs797044555
Varsomers797044555
Maprs797044555
PheGenIrs797044555
hapmaprs797044555
1000 genomesrs797044555
hgdprs797044555
ensemblrs797044555
gopubmedrs797044555
geneviewrs797044555
scholarrs797044555
googlers797044555
pharmgkbrs797044555
gwascentralrs797044555
openSNPrs797044555
23andMers797044555
23andMe allrs797044555
SNP Nexus

SNPshotrs797044555
SNPdbers797044555
MSV3drs797044555
GWAS Ctlgrs797044555
Max Magnitude0
ClinVar
Risk rs797044555(AGGGA;AGGGA)
Alt rs797044555(AGGGA;AGGGA)
Reference Rs797044555(;)
Significance Pathogenic
Disease Mirror movements 1
Variation info
Gene DCC
CLNDBN Mirror movements 1
Reversed 0
HGVS NC_000018.9:g.50929199_50929203dupAGGGA
CLNSRC
CLNACC RCV000192082.1,