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rs121908409

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908409(C;T)
Make rs121908409(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position14871434
GeneANKH
is asnp
is mentioned by
dbSNPrs121908409
ebirs121908409
HLIrs121908409
Exacrs121908409
Varsomers121908409
Maprs121908409
PheGenIrs121908409
hapmaprs121908409
1000 genomesrs121908409
hgdprs121908409
ensemblrs121908409
gopubmedrs121908409
geneviewrs121908409
scholarrs121908409
googlers121908409
pharmgkbrs121908409
gwascentralrs121908409
openSNPrs121908409
23andMers121908409
23andMe allrs121908409
SNP Nexus

SNPshotrs121908409
SNPdbers121908409
MSV3drs121908409
GWAS Ctlgrs121908409
Max Magnitude0
OMIM605145
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121908409(T;T)
Alt rs121908409(T;T)
Reference rs121908409(C;C)
Significance Pathogenic
Disease Chondrocalcinosis 2
Variation info
Gene ANKH
CLNDBN Chondrocalcinosis 2
Reversed 1
HGVS NC_000005.9:g.14871543G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005508.2,