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rs779007169

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779007169(C;G)
Make rs779007169(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position1520177
GeneIFT140
is asnp
is mentioned by
dbSNPrs779007169
ebirs779007169
HLIrs779007169
Exacrs779007169
Varsomers779007169
Maprs779007169
PheGenIrs779007169
hapmaprs779007169
1000 genomesrs779007169
hgdprs779007169
ensemblrs779007169
gopubmedrs779007169
geneviewrs779007169
scholarrs779007169
googlers779007169
pharmgkbrs779007169
gwascentralrs779007169
openSNPrs779007169
23andMers779007169
23andMe allrs779007169
SNP Nexus

SNPshotrs779007169
SNPdbers779007169
MSV3drs779007169
GWAS Ctlgrs779007169
Max Magnitude0
ClinVar
Risk rs779007169(G,T;G,T)
Alt rs779007169(G,T;G,T)
Reference rs779007169(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene IFT140
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000016.9:g.1570178C>T
CLNSRC
CLNACC RCV000201484.1,