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rs398123810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123810(-;-)
Make rs398123810(-;CT)
Make rs398123810(CT;CT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13744461
GeneOFD1
is asnp
is mentioned by
dbSNPrs398123810
ebirs398123810
HLIrs398123810
Exacrs398123810
Varsomers398123810
Maprs398123810
PheGenIrs398123810
hapmaprs398123810
1000 genomesrs398123810
hgdprs398123810
ensemblrs398123810
gopubmedrs398123810
geneviewrs398123810
scholarrs398123810
googlers398123810
pharmgkbrs398123810
gwascentralrs398123810
openSNPrs398123810
23andMers398123810
23andMe allrs398123810
SNP Nexus

SNPshotrs398123810
SNPdbers398123810
MSV3drs398123810
GWAS Ctlgrs398123810
Max Magnitude0
ClinVar
Risk rs398123810(CT;CT)
Alt rs398123810(CT;CT)
Reference rs398123810(;)
Significance Pathogenic
Disease not provided
Variation info
Gene OFD1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.13762579_13762580dupCT
CLNSRC ClinVar
CLNACC RCV000080342.4,