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rs312262891

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs312262891(-;-)
Make rs312262891(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13760636
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262891
ebirs312262891
HLIrs312262891
Exacrs312262891
Varsomers312262891
Maprs312262891
PheGenIrs312262891
hapmaprs312262891
1000 genomesrs312262891
hgdprs312262891
ensemblrs312262891
gopubmedrs312262891
geneviewrs312262891
scholarrs312262891
googlers312262891
pharmgkbrs312262891
gwascentralrs312262891
openSNPrs312262891
23andMers312262891
23andMe allrs312262891
SNP Nexus

SNPshotrs312262891
SNPdbers312262891
MSV3drs312262891
GWAS Ctlgrs312262891
Max Magnitude0
ClinVar
Risk rs312262891(;)
Alt rs312262891(;)
Reference rs312262891(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.13778755delC
CLNSRC ClinVar GeneReviews
CLNACC RCV000033992.2,