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rs797045203

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045203(A;A)
Make rs797045203(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position58909540
GeneGNAS
is asnp
is mentioned by
dbSNPrs797045203
ebirs797045203
HLIrs797045203
Exacrs797045203
Varsomers797045203
Maprs797045203
PheGenIrs797045203
hapmaprs797045203
1000 genomesrs797045203
hgdprs797045203
ensemblrs797045203
gopubmedrs797045203
geneviewrs797045203
scholarrs797045203
googlers797045203
pharmgkbrs797045203
gwascentralrs797045203
openSNPrs797045203
23andMers797045203
23andMe allrs797045203
SNP Nexus

SNPshotrs797045203
SNPdbers797045203
MSV3drs797045203
GWAS Ctlgrs797045203
Max Magnitude0
ClinVar
Risk rs797045203(A;A)
Alt rs797045203(A;A)
Reference rs797045203(C;C)
Significance Pathogenic
Disease McCune-Albright syndrome
Variation info
Gene GNAS
CLNDBN McCune-Albright syndrome
Reversed 0
HGVS NC_000020.10:g.57484595C>A
CLNSRC
CLNACC RCV000191993.1,