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rs312262879

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs312262879(-;-)
Make rs312262879(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13756765
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262879
ebirs312262879
HLIrs312262879
Exacrs312262879
Varsomers312262879
Maprs312262879
PheGenIrs312262879
hapmaprs312262879
1000 genomesrs312262879
hgdprs312262879
ensemblrs312262879
gopubmedrs312262879
geneviewrs312262879
scholarrs312262879
googlers312262879
pharmgkbrs312262879
gwascentralrs312262879
openSNPrs312262879
23andMers312262879
23andMe allrs312262879
SNP Nexus

SNPshotrs312262879
SNPdbers312262879
MSV3drs312262879
GWAS Ctlgrs312262879
Max Magnitude0
ClinVar
Risk rs312262879(;)
Alt rs312262879(;)
Reference rs312262879(A;A)
Significance Pathogenic
Disease Oral-facial-digital syndrome
Variation info
Gene OFD1
CLNDBN Oral-facial-digital syndrome
Reversed 0
HGVS NC_000023.10:g.13774884delA
CLNSRC ClinVar GeneReviews
CLNACC RCV000033978.2,