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rs312262880

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs312262880(C;T)
Make rs312262880(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13757668
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262880
ebirs312262880
HLIrs312262880
Exacrs312262880
Varsomers312262880
Maprs312262880
PheGenIrs312262880
hapmaprs312262880
1000 genomesrs312262880
hgdprs312262880
ensemblrs312262880
gopubmedrs312262880
geneviewrs312262880
scholarrs312262880
googlers312262880
pharmgkbrs312262880
gwascentralrs312262880
openSNPrs312262880
23andMers312262880
23andMe allrs312262880
SNP Nexus

SNPshotrs312262880
SNPdbers312262880
MSV3drs312262880
GWAS Ctlgrs312262880
Max Magnitude0
ClinVar
Risk rs312262880(T;T)
Alt rs312262880(T;T)
Reference rs312262880(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.13775787C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000033979.2,