Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913495

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913495(A;A)
Make rs121913495(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position58909366
GeneGNAS
is asnp
is mentioned by
dbSNPrs121913495
ebirs121913495
HLIrs121913495
Exacrs121913495
Varsomers121913495
Maprs121913495
PheGenIrs121913495
hapmaprs121913495
1000 genomesrs121913495
hgdprs121913495
ensemblrs121913495
gopubmedrs121913495
geneviewrs121913495
scholarrs121913495
googlers121913495
pharmgkbrs121913495
gwascentralrs121913495
openSNPrs121913495
23andMers121913495
23andMe allrs121913495
SNP Nexus

SNPshotrs121913495
SNPdbers121913495
MSV3drs121913495
GWAS Ctlgrs121913495
Max Magnitude0
OMIM139320
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121913495(A,T;A,T)
Alt rs121913495(A,T;A,T)
Reference rs121913495(G;G)
Significance Pathogenic
Disease McCune-Albright syndrome Somatotroph adenoma Cushing's syndrome Sex cord-stromal tumor
Variation info
Gene GNAS
CLNDBN McCune-Albright syndrome Somatotroph adenoma Cushing's syndrome Sex cord-stromal tumor
Reversed 0
HGVS NC_000020.10:g.57484421G>A; NC_000020.10:g.57484421G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017290.4, RCV000017291.4, RCV000017292.4, RCV000017293.4, RCV000191992.1,