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rs587776909

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776909(-;-)
Make rs587776909(-;C)
Make rs587776909(C;C)
ReferenceGRCh38 38.1/142
Chromosome16
Position1520005
GeneIFT140
is asnp
is mentioned by
dbSNPrs587776909
ebirs587776909
HLIrs587776909
Exacrs587776909
Varsomers587776909
Maprs587776909
PheGenIrs587776909
hapmaprs587776909
1000 genomesrs587776909
hgdprs587776909
ensemblrs587776909
gopubmedrs587776909
geneviewrs587776909
scholarrs587776909
googlers587776909
pharmgkbrs587776909
gwascentralrs587776909
openSNPrs587776909
23andMers587776909
23andMe allrs587776909
SNP Nexus

SNPshotrs587776909
SNPdbers587776909
MSV3drs587776909
GWAS Ctlgrs587776909
Max Magnitude0
ClinVar
Risk rs587776909(C;C)
Alt rs587776909(C;C)
Reference rs587776909(;)
Significance Pathogenic
Disease Renal dysplasia
Variation info
Gene IFT140
CLNDBN Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia
Reversed 0
HGVS NC_000016.9:g.1570006dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000024364.3,