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rs727503898

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503898(G;T)
Make rs727503898(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111333096
GeneDCX
is asnp
is mentioned by
dbSNPrs727503898
ebirs727503898
HLIrs727503898
Exacrs727503898
Varsomers727503898
Maprs727503898
PheGenIrs727503898
hapmaprs727503898
1000 genomesrs727503898
hgdprs727503898
ensemblrs727503898
gopubmedrs727503898
geneviewrs727503898
scholarrs727503898
googlers727503898
pharmgkbrs727503898
gwascentralrs727503898
openSNPrs727503898
23andMers727503898
23andMe allrs727503898
SNP Nexus

SNPshotrs727503898
SNPdbers727503898
MSV3drs727503898
GWAS Ctlgrs727503898
Max Magnitude0
ClinVar
Risk rs727503898(T;T)
Alt rs727503898(T;T)
Reference rs727503898(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DCX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.110576324C>A
CLNSRC
CLNACC RCV000153146.3,