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rs267606873

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606873(A;A)
Make rs267606873(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position219057627
GeneIHH
is asnp
is mentioned by
dbSNPrs267606873
ebirs267606873
HLIrs267606873
Exacrs267606873
Varsomers267606873
Maprs267606873
PheGenIrs267606873
hapmaprs267606873
1000 genomesrs267606873
hgdprs267606873
ensemblrs267606873
gopubmedrs267606873
geneviewrs267606873
scholarrs267606873
googlers267606873
pharmgkbrs267606873
gwascentralrs267606873
openSNPrs267606873
23andMers267606873
23andMe allrs267606873
SNP Nexus

SNPshotrs267606873
SNPdbers267606873
MSV3drs267606873
GWAS Ctlgrs267606873
Max Magnitude0
ClinVar
Risk rs267606873(A;A)
Alt rs267606873(A;A)
Reference rs267606873(G;G)
Significance Pathogenic
Disease Brachydactyly type A1
Variation info
Gene IHH
CLNDBN Brachydactyly type A1
Reversed 1
HGVS NC_000002.11:g.219922349C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009425.3,