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rs122460150

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs122460150(A;C)
Make rs122460150(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13756659
GeneOFD1
is asnp
is mentioned by
dbSNPrs122460150
ebirs122460150
HLIrs122460150
Exacrs122460150
Varsomers122460150
Maprs122460150
PheGenIrs122460150
hapmaprs122460150
1000 genomesrs122460150
hgdprs122460150
ensemblrs122460150
gopubmedrs122460150
geneviewrs122460150
scholarrs122460150
googlers122460150
pharmgkbrs122460150
gwascentralrs122460150
openSNPrs122460150
23andMers122460150
23andMe allrs122460150
SNP Nexus

SNPshotrs122460150
SNPdbers122460150
MSV3drs122460150
GWAS Ctlgrs122460150
Max Magnitude0
OMIM300170
Desc
Variant0001
Relatedalso
ClinVar
Risk rs122460150(C;C)
Alt rs122460150(C;C)
Reference rs122460150(A;A)
Significance Pathogenic
Disease Oral-facial-digital syndrome
Variation info
Gene OFD1
CLNDBN Oral-facial-digital syndrome
Reversed 0
HGVS NC_000023.10:g.13774778A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012293.25,