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rs312262885

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs312262885(-;-)
Make rs312262885(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13760281
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262885
ebirs312262885
HLIrs312262885
Exacrs312262885
Varsomers312262885
Maprs312262885
PheGenIrs312262885
hapmaprs312262885
1000 genomesrs312262885
hgdprs312262885
ensemblrs312262885
gopubmedrs312262885
geneviewrs312262885
scholarrs312262885
googlers312262885
pharmgkbrs312262885
gwascentralrs312262885
openSNPrs312262885
23andMers312262885
23andMe allrs312262885
SNP Nexus

SNPshotrs312262885
SNPdbers312262885
MSV3drs312262885
GWAS Ctlgrs312262885
Max Magnitude0
ClinVar
Risk rs312262885(;)
Alt rs312262885(;)
Reference rs312262885(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.13778400delG
CLNSRC ClinVar GeneReviews
CLNACC RCV000033985.2,