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rs1064795798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome20
Position58910780
GeneGNAS
is asnp
is mentioned by
dbSNPrs1064795798
dbSNP (old)rs1064795798
ClinGenrs1064795798
ebirs1064795798
HLIrs1064795798
Exacrs1064795798
Gnomadrs1064795798
Varsomers1064795798
Maprs1064795798
PheGenIrs1064795798
Biobankrs1064795798
1000 genomesrs1064795798
hgdprs1064795798
ensemblrs1064795798
gopubmedrs1064795798
geneviewrs1064795798
scholarrs1064795798
googlers1064795798
pharmgkbrs1064795798
gwascentralrs1064795798
openSNPrs1064795798
23andMers1064795798
23andMe allrs1064795798
SNPshotrs1064795798
SNPdbers1064795798
MSV3drs1064795798
GWAS Ctlgrs1064795798
Max Magnitude0
ClinVar
Risk rs1064795798(A;A)
Alt rs1064795798(A;A)
Reference Rs1064795798(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GNAS
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.57485835G>A
CLNSRC
CLNACC RCV000481496.1,