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rs387906787

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906787(C;T)
Make rs387906787(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34657331
GeneIL11RA
is asnp
is mentioned by
dbSNPrs387906787
ebirs387906787
HLIrs387906787
Exacrs387906787
Varsomers387906787
Maprs387906787
PheGenIrs387906787
hapmaprs387906787
1000 genomesrs387906787
hgdprs387906787
ensemblrs387906787
gopubmedrs387906787
geneviewrs387906787
scholarrs387906787
googlers387906787
pharmgkbrs387906787
gwascentralrs387906787
openSNPrs387906787
23andMers387906787
23andMe allrs387906787
SNP Nexus

SNPshotrs387906787
SNPdbers387906787
MSV3drs387906787
GWAS Ctlgrs387906787
Max Magnitude0
ClinVar
Risk rs387906787(T;T)
Alt rs387906787(T;T)
Reference rs387906787(C;C)
Significance Pathogenic
Disease Craniosynostosis and dental anomalies
Variation info
Gene IL11RA
CLNDBN Craniosynostosis and dental anomalies
Reversed 0
HGVS NC_000009.11:g.34657328C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023050.2,