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rs312262889

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs312262889(-;-)
Make rs312262889(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13760516
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262889
ebirs312262889
HLIrs312262889
Exacrs312262889
Varsomers312262889
Maprs312262889
PheGenIrs312262889
hapmaprs312262889
1000 genomesrs312262889
hgdprs312262889
ensemblrs312262889
gopubmedrs312262889
geneviewrs312262889
scholarrs312262889
googlers312262889
pharmgkbrs312262889
gwascentralrs312262889
openSNPrs312262889
23andMers312262889
23andMe allrs312262889
SNP Nexus

SNPshotrs312262889
SNPdbers312262889
MSV3drs312262889
GWAS Ctlgrs312262889
Max Magnitude0
ClinVar
Risk rs312262889(;)
Alt rs312262889(;)
Reference rs312262889(T;T)
Significance Pathogenic
Disease Oral-facial-digital syndrome
Variation info
Gene OFD1
CLNDBN Oral-facial-digital syndrome
Reversed 0
HGVS NC_000023.10:g.13778635delT
CLNSRC ClinVar GeneReviews
CLNACC RCV000033990.2,