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rs121917859

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121917859(A;G)
Make rs121917859(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position219060184
GeneIHH
is asnp
is mentioned by
dbSNPrs121917859
ebirs121917859
HLIrs121917859
Exacrs121917859
Varsomers121917859
Maprs121917859
PheGenIrs121917859
hapmaprs121917859
1000 genomesrs121917859
hgdprs121917859
ensemblrs121917859
gopubmedrs121917859
geneviewrs121917859
scholarrs121917859
googlers121917859
pharmgkbrs121917859
gwascentralrs121917859
openSNPrs121917859
23andMers121917859
23andMe allrs121917859
SNP Nexus

SNPshotrs121917859
SNPdbers121917859
MSV3drs121917859
GWAS Ctlgrs121917859
Max Magnitude0
ClinVar
Risk rs121917859(G;G)
Alt rs121917859(G;G)
Reference rs121917859(A;A)
Significance Pathogenic
Disease Brachydactyly type A1
Variation info
Gene IHH MIR3131
CLNDBN Brachydactyly type A1
Reversed 1
HGVS NC_000002.11:g.219924906T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009422.3,