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rs797044556

From SNPedia

Orientationplus
Make rs797044556(-;-)
Make rs797044556(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position53486895
GeneDCC
is asnp
is mentioned by
dbSNPrs797044556
ebirs797044556
HLIrs797044556
Exacrs797044556
Varsomers797044556
Maprs797044556
PheGenIrs797044556
hapmaprs797044556
1000 genomesrs797044556
hgdprs797044556
ensemblrs797044556
gopubmedrs797044556
geneviewrs797044556
scholarrs797044556
googlers797044556
pharmgkbrs797044556
gwascentralrs797044556
openSNPrs797044556
23andMers797044556
23andMe allrs797044556
SNP Nexus

SNPshotrs797044556
SNPdbers797044556
MSV3drs797044556
GWAS Ctlgrs797044556
Max Magnitude
ClinVar
Risk rs797044556(;)
Alt rs797044556(;)
Reference rs797044556(CT;CT)
Significance Pathogenic
Disease Mirror movements
Variation info
Gene DCC
CLNDBN Mirror movements, congenital
Reversed 0
HGVS NC_000018.9:g.51013265_51013266delCT
CLNSRC
CLNACC RCV000192083.1,