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rs786205858

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205858(A;A)
Make rs786205858(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position27457760
GeneIFT172
is asnp
is mentioned by
dbSNPrs786205858
ebirs786205858
HLIrs786205858
Exacrs786205858
Varsomers786205858
Maprs786205858
PheGenIrs786205858
hapmaprs786205858
1000 genomesrs786205858
hgdprs786205858
ensemblrs786205858
gopubmedrs786205858
geneviewrs786205858
scholarrs786205858
googlers786205858
pharmgkbrs786205858
gwascentralrs786205858
openSNPrs786205858
23andMers786205858
23andMe allrs786205858
SNP Nexus

SNPshotrs786205858
SNPdbers786205858
MSV3drs786205858
GWAS Ctlgrs786205858
Max Magnitude0
ClinVar
Risk rs786205858(A;A)
Alt rs786205858(A;A)
Reference rs786205858(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 71
Variation info
Gene IFT172
CLNDBN Retinitis pigmentosa 71
Reversed 1
HGVS NC_000002.11:g.27680627A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000171552.2,