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rs312262868

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AATC;AATC) 0 common in clinvar
(TCAA;TCAA) 0 common in clinvar
Make rs312262868(-;-)
Make rs312262868(-;AATC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13755214
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262868
ebirs312262868
HLIrs312262868
Exacrs312262868
Varsomers312262868
Maprs312262868
PheGenIrs312262868
hapmaprs312262868
1000 genomesrs312262868
hgdprs312262868
ensemblrs312262868
gopubmedrs312262868
geneviewrs312262868
scholarrs312262868
googlers312262868
pharmgkbrs312262868
gwascentralrs312262868
openSNPrs312262868
23andMers312262868
23andMe allrs312262868
SNP Nexus

SNPshotrs312262868
SNPdbers312262868
MSV3drs312262868
GWAS Ctlgrs312262868
Max Magnitude0
ClinVar
Risk rs312262868(;)
Alt rs312262868(;)
Reference rs312262868(TCAA;TCAA)
Significance Pathogenic
Disease Oral-facial-digital syndrome not provided
Variation info
Gene OFD1
CLNDBN Oral-facial-digital syndrome not provided
Reversed 0
HGVS NC_000023.10:g.13773333_13773336delAATC
CLNSRC ClinVar GeneReviews University of Chicago
CLNACC RCV000033964.2, RCV000146976.1,