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rs312262826

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs312262826(C;G)
Make rs312262826(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13738905
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262826
ebirs312262826
HLIrs312262826
Exacrs312262826
Varsomers312262826
Maprs312262826
PheGenIrs312262826
hapmaprs312262826
1000 genomesrs312262826
hgdprs312262826
ensemblrs312262826
gopubmedrs312262826
geneviewrs312262826
scholarrs312262826
googlers312262826
pharmgkbrs312262826
gwascentralrs312262826
openSNPrs312262826
23andMers312262826
23andMe allrs312262826
SNP Nexus

SNPshotrs312262826
SNPdbers312262826
MSV3drs312262826
GWAS Ctlgrs312262826
Max Magnitude0
ClinVar
Risk rs312262826(G;G)
Alt rs312262826(G;G)
Reference rs312262826(C;C)
Significance Pathogenic
Disease Oral-facial-digital syndrome
Variation info
Gene OFD1
CLNDBN Oral-facial-digital syndrome
Reversed 0
HGVS NC_000023.10:g.13757024C>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000034012.2,