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rs398123809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123809(A;C)
Make rs398123809(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13758335
GeneOFD1
is asnp
is mentioned by
dbSNPrs398123809
ebirs398123809
HLIrs398123809
Exacrs398123809
Varsomers398123809
Maprs398123809
PheGenIrs398123809
hapmaprs398123809
1000 genomesrs398123809
hgdprs398123809
ensemblrs398123809
gopubmedrs398123809
geneviewrs398123809
scholarrs398123809
googlers398123809
pharmgkbrs398123809
gwascentralrs398123809
openSNPrs398123809
23andMers398123809
23andMe allrs398123809
SNP Nexus

SNPshotrs398123809
SNPdbers398123809
MSV3drs398123809
GWAS Ctlgrs398123809
Max Magnitude0
ClinVar
Risk rs398123809(C;C)
Alt rs398123809(C;C)
Reference rs398123809(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OFD1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.13776454A>C
CLNSRC ClinVar
CLNACC RCV000080340.4,