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rs312262836

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs312262836(C;T)
Make rs312262836(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13744456
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262836
ebirs312262836
HLIrs312262836
Exacrs312262836
Varsomers312262836
Maprs312262836
PheGenIrs312262836
hapmaprs312262836
1000 genomesrs312262836
hgdprs312262836
ensemblrs312262836
gopubmedrs312262836
geneviewrs312262836
scholarrs312262836
googlers312262836
pharmgkbrs312262836
gwascentralrs312262836
openSNPrs312262836
23andMers312262836
23andMe allrs312262836
SNP Nexus

SNPshotrs312262836
SNPdbers312262836
MSV3drs312262836
GWAS Ctlgrs312262836
Max Magnitude0
ClinVar
Risk rs312262836(T;T)
Alt rs312262836(T;T)
Reference rs312262836(C;C)
Significance Pathogenic
Disease Oral-facial-digital syndrome
Variation info
Gene OFD1
CLNDBN Oral-facial-digital syndrome
Reversed 0
HGVS NC_000023.10:g.13762575C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034025.2,