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rs201870761

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs201870761(C;C)
Make rs201870761(C;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position111410089
GeneDCX
is asnp
is mentioned by
dbSNPrs201870761
ebirs201870761
HLIrs201870761
Exacrs201870761
Varsomers201870761
Maprs201870761
PheGenIrs201870761
hapmaprs201870761
1000 genomesrs201870761
hgdprs201870761
ensemblrs201870761
gopubmedrs201870761
geneviewrs201870761
scholarrs201870761
googlers201870761
pharmgkbrs201870761
gwascentralrs201870761
openSNPrs201870761
23andMers201870761
23andMe allrs201870761
SNP Nexus

SNPshotrs201870761
SNPdbers201870761
MSV3drs201870761
GWAS Ctlgrs201870761
Max Magnitude0
ClinVar
Risk rs201870761(A,C;A,C)
Alt rs201870761(A,C;A,C)
Reference rs201870761(T;T)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 0
HGVS NC_000023.10:g.110653317T>A
CLNSRC ClinVar University of Chicago
CLNACC RCV000145835.1,