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rs312262822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs312262822(-;-)
Make rs312262822(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13736678
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262822
ebirs312262822
HLIrs312262822
Exacrs312262822
Varsomers312262822
Maprs312262822
PheGenIrs312262822
hapmaprs312262822
1000 genomesrs312262822
hgdprs312262822
ensemblrs312262822
gopubmedrs312262822
geneviewrs312262822
scholarrs312262822
googlers312262822
pharmgkbrs312262822
gwascentralrs312262822
openSNPrs312262822
23andMers312262822
23andMe allrs312262822
SNP Nexus

SNPshotrs312262822
SNPdbers312262822
MSV3drs312262822
GWAS Ctlgrs312262822
Max Magnitude0
ClinVar
Risk rs312262822(;)
Alt rs312262822(;)
Reference rs312262822(G;G)
Significance Pathogenic
Disease Oral-facial-digital syndrome
Variation info
Gene OFD1
CLNDBN Oral-facial-digital syndrome
Reversed 0
HGVS NC_000023.10:g.13754797delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000012294.25,