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rs387906784

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906784(C;T)
Make rs387906784(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34659834
GeneIL11RA
is asnp
is mentioned by
dbSNPrs387906784
ebirs387906784
HLIrs387906784
Exacrs387906784
Varsomers387906784
Maprs387906784
PheGenIrs387906784
hapmaprs387906784
1000 genomesrs387906784
hgdprs387906784
ensemblrs387906784
gopubmedrs387906784
geneviewrs387906784
scholarrs387906784
googlers387906784
pharmgkbrs387906784
gwascentralrs387906784
openSNPrs387906784
23andMers387906784
23andMe allrs387906784
SNP Nexus

SNPshotrs387906784
SNPdbers387906784
MSV3drs387906784
GWAS Ctlgrs387906784
Max Magnitude0
ClinVar
Risk rs387906784(T;T)
Alt rs387906784(T;T)
Reference rs387906784(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.34659831C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023047.2,