Have questions? Visit https://www.reddit.com/r/SNPedia

rs762081862

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs762081862(A;A)
Make rs762081862(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position58458545
GeneKIAA0586
is asnp
is mentioned by
dbSNPrs762081862
ebirs762081862
HLIrs762081862
Exacrs762081862
Varsomers762081862
Maprs762081862
PheGenIrs762081862
hapmaprs762081862
1000 genomesrs762081862
hgdprs762081862
ensemblrs762081862
gopubmedrs762081862
geneviewrs762081862
scholarrs762081862
googlers762081862
pharmgkbrs762081862
gwascentralrs762081862
openSNPrs762081862
23andMers762081862
23andMe allrs762081862
SNP Nexus

SNPshotrs762081862
SNPdbers762081862
MSV3drs762081862
GWAS Ctlgrs762081862
Max Magnitude0
ClinVar
Risk rs762081862(A;A)
Alt rs762081862(A;A)
Reference rs762081862(G;G)
Significance Pathogenic
Disease Short-rib thoracic dysplasia 14 with polydactyly
Variation info
Gene KIAA0586
CLNDBN Short-rib thoracic dysplasia 14 with polydactyly
Reversed 0
HGVS NC_000014.8:g.58925263G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190841.3,