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rs111541229

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111541229(C;C)
Make rs111541229(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position58898986
GeneGNAS
is asnp
is mentioned by
dbSNPrs111541229
dbSNP (classic)rs111541229
ClinGenrs111541229
ebirs111541229
HLIrs111541229
Exacrs111541229
Gnomadrs111541229
Varsomers111541229
LitVarrs111541229
Maprs111541229
PheGenIrs111541229
Biobankrs111541229
1000 genomesrs111541229
hgdprs111541229
ensemblrs111541229
geneviewrs111541229
scholarrs111541229
googlers111541229
pharmgkbrs111541229
gwascentralrs111541229
openSNPrs111541229
23andMers111541229
23andMe allrs111541229
SNPshotrs111541229
SNPdbers111541229
MSV3drs111541229
GWAS Ctlgrs111541229
Max Magnitude0
ClinVar
Risk rs111541229(C;C) rs111541229(T;T)
Alt rs111541229(C;C) rs111541229(T;T)
Reference Rs111541229(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GNAS
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.57474041G>T
CLNSRC
CLNACC RCV000482442.1,