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rs312262892

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs312262892(G;T)
Make rs312262892(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13761084
GeneOFD1
is asnp
is mentioned by
dbSNPrs312262892
ebirs312262892
HLIrs312262892
Exacrs312262892
Varsomers312262892
Maprs312262892
PheGenIrs312262892
hapmaprs312262892
1000 genomesrs312262892
hgdprs312262892
ensemblrs312262892
gopubmedrs312262892
geneviewrs312262892
scholarrs312262892
googlers312262892
pharmgkbrs312262892
gwascentralrs312262892
openSNPrs312262892
23andMers312262892
23andMe allrs312262892
SNP Nexus

SNPshotrs312262892
SNPdbers312262892
MSV3drs312262892
GWAS Ctlgrs312262892
Max Magnitude0
ClinVar
Risk rs312262892(T;T)
Alt rs312262892(T;T)
Reference rs312262892(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.13779203G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000033995.2,