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rs11806366

From SNPedia

Orientationplus
Stabilizedplus
Make rs11806366(C;C)
Make rs11806366(C;G)
Make rs11806366(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position8923596
is asnp
is mentioned by
dbSNPrs11806366
dbSNP (old)rs11806366
ClinGenrs11806366
ebirs11806366
HLIrs11806366
Exacrs11806366
Gnomadrs11806366
Varsomers11806366
Maprs11806366
PheGenIrs11806366
Biobankrs11806366
1000 genomesrs11806366
hgdprs11806366
ensemblrs11806366
gopubmedrs11806366
geneviewrs11806366
scholarrs11806366
googlers11806366
pharmgkbrs11806366
gwascentralrs11806366
openSNPrs11806366
23andMers11806366
23andMe allrs11806366
SNP Nexus

SNPshotrs11806366
SNPdbers11806366
MSV3drs11806366
GWAS Ctlgrs11806366
GMAF0.3747
Max Magnitude
? (C;C) (C;G) (G;G) 28
OMIM613328
DescROIFMAN-CHITAYAT SYNDROME
Variant
Relatedalso