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rs121908410

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908410(A;A)
Make rs121908410(A;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position14871435
GeneANKH
is asnp
is mentioned by
dbSNPrs121908410
ebirs121908410
HLIrs121908410
Exacrs121908410
Varsomers121908410
Maprs121908410
PheGenIrs121908410
hapmaprs121908410
1000 genomesrs121908410
hgdprs121908410
ensemblrs121908410
gopubmedrs121908410
geneviewrs121908410
scholarrs121908410
googlers121908410
pharmgkbrs121908410
gwascentralrs121908410
openSNPrs121908410
23andMers121908410
23andMe allrs121908410
SNP Nexus

SNPshotrs121908410
SNPdbers121908410
MSV3drs121908410
GWAS Ctlgrs121908410
Max Magnitude0
OMIM605145
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121908410(A;A)
Alt rs121908410(A;A)
Reference rs121908410(C;C)
Significance Pathogenic
Disease Chondrocalcinosis 2
Variation info
Gene ANKH
CLNDBN Chondrocalcinosis 2
Reversed 1
HGVS NC_000005.9:g.14871544G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005509.2,