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rs786205566

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205566(G;T)
Make rs786205566(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position129483546
GeneIFT122
is asnp
is mentioned by
dbSNPrs786205566
ebirs786205566
HLIrs786205566
Exacrs786205566
Varsomers786205566
Maprs786205566
PheGenIrs786205566
hapmaprs786205566
1000 genomesrs786205566
hgdprs786205566
ensemblrs786205566
gopubmedrs786205566
geneviewrs786205566
scholarrs786205566
googlers786205566
pharmgkbrs786205566
gwascentralrs786205566
openSNPrs786205566
23andMers786205566
23andMe allrs786205566
SNP Nexus

SNPshotrs786205566
SNPdbers786205566
MSV3drs786205566
GWAS Ctlgrs786205566
Max Magnitude0
ClinVar
Risk rs786205566(T;T)
Alt rs786205566(T;T)
Reference rs786205566(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IFT122
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.129202389G>T
CLNSRC
CLNACC RCV000171370.1,