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rs121917856

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917856(C;T)
Make rs121917856(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position219060331
GeneIHH
is asnp
is mentioned by
dbSNPrs121917856
ebirs121917856
HLIrs121917856
Exacrs121917856
Varsomers121917856
Maprs121917856
PheGenIrs121917856
hapmaprs121917856
1000 genomesrs121917856
hgdprs121917856
ensemblrs121917856
gopubmedrs121917856
geneviewrs121917856
scholarrs121917856
googlers121917856
pharmgkbrs121917856
gwascentralrs121917856
openSNPrs121917856
23andMers121917856
23andMe allrs121917856
SNP Nexus

SNPshotrs121917856
SNPdbers121917856
MSV3drs121917856
GWAS Ctlgrs121917856
Max Magnitude0
ClinVar
Risk rs121917856(T;T)
Alt rs121917856(T;T)
Reference rs121917856(C;C)
Significance Pathogenic
Disease Acrocapitofemoral dysplasia
Variation info
Gene IHH MIR3131
CLNDBN Acrocapitofemoral dysplasia
Reversed 1
HGVS NC_000002.11:g.219925053G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009420.3,