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

rs1057520715

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520715(A;A)
Make rs1057520715(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position58891851
GeneGNAS
is asnp
is mentioned by
dbSNPrs1057520715
dbSNP (old)rs1057520715
ClinGenrs1057520715
ebirs1057520715
HLIrs1057520715
Exacrs1057520715
Gnomadrs1057520715
Varsomers1057520715
Maprs1057520715
PheGenIrs1057520715
Biobankrs1057520715
1000 genomesrs1057520715
hgdprs1057520715
ensemblrs1057520715
gopubmedrs1057520715
geneviewrs1057520715
scholarrs1057520715
googlers1057520715
pharmgkbrs1057520715
gwascentralrs1057520715
openSNPrs1057520715
23andMers1057520715
23andMe allrs1057520715
SNPshotrs1057520715
SNPdbers1057520715
MSV3drs1057520715
GWAS Ctlgrs1057520715
Max Magnitude0
ClinVar
Risk rs1057520715(A;A)
Alt rs1057520715(A;A)
Reference Rs1057520715(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GNAS
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.57466906G>A
CLNSRC
CLNACC RCV000429080.1,