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rs312262893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs312262893(-;-)
Make rs312262893(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13761173
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262893
ebirs312262893
HLIrs312262893
Exacrs312262893
Varsomers312262893
Maprs312262893
PheGenIrs312262893
hapmaprs312262893
1000 genomesrs312262893
hgdprs312262893
ensemblrs312262893
gopubmedrs312262893
geneviewrs312262893
scholarrs312262893
googlers312262893
pharmgkbrs312262893
gwascentralrs312262893
openSNPrs312262893
23andMers312262893
23andMe allrs312262893
SNP Nexus

SNPshotrs312262893
SNPdbers312262893
MSV3drs312262893
GWAS Ctlgrs312262893
Max Magnitude0
ClinVar
Risk rs312262893(;)
Alt rs312262893(;)
Reference rs312262893(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.13779292delC
CLNSRC ClinVar GeneReviews
CLNACC RCV000033997.2,