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rs121917861

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917861(C;T)
Make rs121917861(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position219057549
GeneIHH
is asnp
is mentioned by
dbSNPrs121917861
ebirs121917861
HLIrs121917861
Exacrs121917861
Varsomers121917861
Maprs121917861
PheGenIrs121917861
hapmaprs121917861
1000 genomesrs121917861
hgdprs121917861
ensemblrs121917861
gopubmedrs121917861
geneviewrs121917861
scholarrs121917861
googlers121917861
pharmgkbrs121917861
gwascentralrs121917861
openSNPrs121917861
23andMers121917861
23andMe allrs121917861
SNP Nexus

SNPshotrs121917861
SNPdbers121917861
MSV3drs121917861
GWAS Ctlgrs121917861
Max Magnitude0
ClinVar
Risk rs121917861(T;T)
Alt rs121917861(T;T)
Reference rs121917861(C;C)
Significance Pathogenic
Disease Brachydactyly type A1
Variation info
Gene IHH
CLNDBN Brachydactyly type A1
Reversed 1
HGVS NC_000002.11:g.219922271G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009423.3,