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rs312262886

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs312262886(-;-)
Make rs312262886(-;AT)
Make rs312262886(AT;AT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13760347
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262886
ebirs312262886
HLIrs312262886
Exacrs312262886
Varsomers312262886
Maprs312262886
PheGenIrs312262886
hapmaprs312262886
1000 genomesrs312262886
hgdprs312262886
ensemblrs312262886
gopubmedrs312262886
geneviewrs312262886
scholarrs312262886
googlers312262886
pharmgkbrs312262886
gwascentralrs312262886
openSNPrs312262886
23andMers312262886
23andMe allrs312262886
SNP Nexus

SNPshotrs312262886
SNPdbers312262886
MSV3drs312262886
GWAS Ctlgrs312262886
Max Magnitude0
ClinVar
Risk rs312262886(AT;AT)
Alt rs312262886(AT;AT)
Reference rs312262886(;)
Significance Pathogenic
Disease Oral-facial-digital syndrome
Variation info
Gene OFD1
CLNDBN Oral-facial-digital syndrome
Reversed 0
HGVS NC_000023.10:g.13778466_13778467insAT
CLNSRC OMIM Allelic Variant
CLNACC RCV000012297.12,