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rs387906786

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906786(C;G)
Make rs387906786(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34658607
GeneIL11RA
is asnp
is mentioned by
dbSNPrs387906786
ebirs387906786
HLIrs387906786
Exacrs387906786
Varsomers387906786
Maprs387906786
PheGenIrs387906786
hapmaprs387906786
1000 genomesrs387906786
hgdprs387906786
ensemblrs387906786
gopubmedrs387906786
geneviewrs387906786
scholarrs387906786
googlers387906786
pharmgkbrs387906786
gwascentralrs387906786
openSNPrs387906786
23andMers387906786
23andMe allrs387906786
SNP Nexus

SNPshotrs387906786
SNPdbers387906786
MSV3drs387906786
GWAS Ctlgrs387906786
Max Magnitude0
ClinVar
Risk rs387906786(G;G)
Alt rs387906786(G;G)
Reference rs387906786(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.34658604C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023049.3,