Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606872

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606872(A;A)
Make rs267606872(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position219057621
GeneIHH
is asnp
is mentioned by
dbSNPrs267606872
ebirs267606872
HLIrs267606872
Exacrs267606872
Varsomers267606872
Maprs267606872
PheGenIrs267606872
hapmaprs267606872
1000 genomesrs267606872
hgdprs267606872
ensemblrs267606872
gopubmedrs267606872
geneviewrs267606872
scholarrs267606872
googlers267606872
pharmgkbrs267606872
gwascentralrs267606872
openSNPrs267606872
23andMers267606872
23andMe allrs267606872
SNP Nexus

SNPshotrs267606872
SNPdbers267606872
MSV3drs267606872
GWAS Ctlgrs267606872
Max Magnitude0
ClinVar
Risk rs267606872(A;A)
Alt rs267606872(A;A)
Reference rs267606872(C;C)
Significance Pathogenic
Disease Brachydactyly type A1
Variation info
Gene IHH
CLNDBN Brachydactyly type A1
Reversed 1
HGVS NC_000002.11:g.219922343G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009426.2,