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rs587777086

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777086(-;-)
Make rs587777086(-;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position27461794
GeneIFT172
is asnp
is mentioned by
dbSNPrs587777086
ebirs587777086
HLIrs587777086
Exacrs587777086
Varsomers587777086
Maprs587777086
PheGenIrs587777086
hapmaprs587777086
1000 genomesrs587777086
hgdprs587777086
ensemblrs587777086
gopubmedrs587777086
geneviewrs587777086
scholarrs587777086
googlers587777086
pharmgkbrs587777086
gwascentralrs587777086
openSNPrs587777086
23andMers587777086
23andMe allrs587777086
SNP Nexus

SNPshotrs587777086
SNPdbers587777086
MSV3drs587777086
GWAS Ctlgrs587777086
Max Magnitude0
ClinVar
Risk rs587777086(GG,G;GG,G)
Alt rs587777086(GG,G;GG,G)
Reference rs587777086(CG;CG)
Significance Pathogenic
Disease Short-rib thoracic dysplasia 10 without polydactyly
Variation info
Gene IFT172
CLNDBN Short-rib thoracic dysplasia 10 without polydactyly
Reversed 1
HGVS NC_000002.11:g.27684661delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000083278.4,