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rs1057518224

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518224(-;-)
Make rs1057518224(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position58910737
GeneGNAS
is asnp
is mentioned by
dbSNPrs1057518224
dbSNP (old)rs1057518224
ClinGenrs1057518224
ebirs1057518224
HLIrs1057518224
Exacrs1057518224
Gnomadrs1057518224
Varsomers1057518224
LitVarrs1057518224
Maprs1057518224
PheGenIrs1057518224
Biobankrs1057518224
1000 genomesrs1057518224
hgdprs1057518224
ensemblrs1057518224
gopubmedrs1057518224
geneviewrs1057518224
scholarrs1057518224
googlers1057518224
pharmgkbrs1057518224
gwascentralrs1057518224
openSNPrs1057518224
23andMers1057518224
23andMe allrs1057518224
SNPshotrs1057518224
SNPdbers1057518224
MSV3drs1057518224
GWAS Ctlgrs1057518224
Max Magnitude0
ClinVar
Risk rs1057518224(-;-)
Alt rs1057518224(-;-)
Reference Rs1057518224(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene GNAS
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.57485792delT
CLNSRC
CLNACC RCV000414072.1,