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

rs797044895

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044895(A;G)
Make rs797044895(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position58895635
GeneGNAS
is asnp
is mentioned by
dbSNPrs797044895
ebirs797044895
HLIrs797044895
Exacrs797044895
Varsomers797044895
Maprs797044895
PheGenIrs797044895
hapmaprs797044895
1000 genomesrs797044895
hgdprs797044895
ensemblrs797044895
gopubmedrs797044895
geneviewrs797044895
scholarrs797044895
googlers797044895
pharmgkbrs797044895
gwascentralrs797044895
openSNPrs797044895
23andMers797044895
23andMe allrs797044895
SNP Nexus

SNPshotrs797044895
SNPdbers797044895
MSV3drs797044895
GWAS Ctlgrs797044895
Max Magnitude0
ClinVar
Risk rs797044895(G;G)
Alt rs797044895(G;G)
Reference rs797044895(A;A)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene GNAS
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000020.10:g.57470690A>G
CLNSRC
CLNACC RCV000190719.1,