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rs797044917

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044917(C;C)
Make rs797044917(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position13749527
GeneOFD1
is asnp
is mentioned by
dbSNPrs797044917
ebirs797044917
HLIrs797044917
Exacrs797044917
Varsomers797044917
Maprs797044917
PheGenIrs797044917
hapmaprs797044917
1000 genomesrs797044917
hgdprs797044917
ensemblrs797044917
gopubmedrs797044917
geneviewrs797044917
scholarrs797044917
googlers797044917
pharmgkbrs797044917
gwascentralrs797044917
openSNPrs797044917
23andMers797044917
23andMe allrs797044917
SNP Nexus

SNPshotrs797044917
SNPdbers797044917
MSV3drs797044917
GWAS Ctlgrs797044917
Max Magnitude0
ClinVar
Risk rs797044917(C;C)
Alt rs797044917(C;C)
Reference rs797044917(T;T)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene OFD1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000023.10:g.13767646T>C
CLNSRC
CLNACC RCV000190751.1,