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rs387906785

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906785(C;G)
Make rs387906785(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34658535
GeneIL11RA
is asnp
is mentioned by
dbSNPrs387906785
ebirs387906785
HLIrs387906785
Exacrs387906785
Varsomers387906785
Maprs387906785
PheGenIrs387906785
hapmaprs387906785
1000 genomesrs387906785
hgdprs387906785
ensemblrs387906785
gopubmedrs387906785
geneviewrs387906785
scholarrs387906785
googlers387906785
pharmgkbrs387906785
gwascentralrs387906785
openSNPrs387906785
23andMers387906785
23andMe allrs387906785
SNP Nexus

SNPshotrs387906785
SNPdbers387906785
MSV3drs387906785
GWAS Ctlgrs387906785
Max Magnitude0
ClinVar
Risk rs387906785(G;G)
Alt rs387906785(G;G)
Reference rs387906785(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.34658532C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023048.2,