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rs312262866

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs312262866(-;A)
Make rs312262866(A;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13755199
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262866
dbSNP (classic)rs312262866
ClinGenrs312262866
ebirs312262866
HLIrs312262866
Exacrs312262866
Gnomadrs312262866
Varsomers312262866
LitVarrs312262866
Maprs312262866
PheGenIrs312262866
Biobankrs312262866
1000 genomesrs312262866
hgdprs312262866
ensemblrs312262866
geneviewrs312262866
scholarrs312262866
googlers312262866
pharmgkbrs312262866
gwascentralrs312262866
openSNPrs312262866
23andMers312262866
SNPshotrs312262866
SNPdbers312262866
MSV3drs312262866
GWAS Ctlgrs312262866
Max Magnitude0
ClinVar
Risk rs312262866(A;A)
Alt rs312262866(A;A)
Reference Rs312262866(-;-)
Significance Pathogenic
Disease Oral-facial-digital syndrome
Variation info
Gene OFD1
CLNDBN Oral-facial-digital syndrome
Reversed 0
HGVS NC_000023.10:g.13773318dupA
CLNSRC ClinVar GeneReviews
CLNACC RCV000033962.2,