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

rs121912588

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121912588(C;C)
Make rs121912588(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position39358326
GeneKIF21A
is asnp
is mentioned by
dbSNPrs121912588
ebirs121912588
HLIrs121912588
Exacrs121912588
Varsomers121912588
Maprs121912588
PheGenIrs121912588
hapmaprs121912588
1000 genomesrs121912588
hgdprs121912588
ensemblrs121912588
gopubmedrs121912588
geneviewrs121912588
scholarrs121912588
googlers121912588
pharmgkbrs121912588
gwascentralrs121912588
openSNPrs121912588
23andMers121912588
23andMe allrs121912588
SNP Nexus

SNPshotrs121912588
SNPdbers121912588
MSV3drs121912588
GWAS Ctlgrs121912588
Max Magnitude0
OMIM608283
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121912588(C;C)
Alt rs121912588(C;C)
Reference rs121912588(T;T)
Significance Pathogenic
Disease Fibrosis of extraocular muscles
Variation info
Gene KIF21A
CLNDBN Fibrosis of extraocular muscles, congenital, 1
Reversed 1
HGVS NC_000012.11:g.39752128A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002543.2,