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rs312262881

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs312262881(-;-)
Make rs312262881(-;TT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13757693
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262881
ebirs312262881
HLIrs312262881
Exacrs312262881
Varsomers312262881
Maprs312262881
PheGenIrs312262881
hapmaprs312262881
1000 genomesrs312262881
hgdprs312262881
ensemblrs312262881
gopubmedrs312262881
geneviewrs312262881
scholarrs312262881
googlers312262881
pharmgkbrs312262881
gwascentralrs312262881
openSNPrs312262881
23andMers312262881
23andMe allrs312262881
SNP Nexus

SNPshotrs312262881
SNPdbers312262881
MSV3drs312262881
GWAS Ctlgrs312262881
Max Magnitude0
ClinVar
Risk rs312262881(;)
Alt rs312262881(;)
Reference rs312262881(TT;TT)
Significance Pathogenic
Disease Oral-facial-digital syndrome
Variation info
Gene OFD1
CLNDBN Oral-facial-digital syndrome
Reversed 0
HGVS NC_000023.10:g.13775812_13775813delTT
CLNSRC ClinVar GeneReviews
CLNACC RCV000033980.2,