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rs137854535

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854535(C;T)
Make rs137854535(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position58909737
GeneGNAS
is asnp
is mentioned by
dbSNPrs137854535
ebirs137854535
HLIrs137854535
Exacrs137854535
Varsomers137854535
Maprs137854535
PheGenIrs137854535
hapmaprs137854535
1000 genomesrs137854535
hgdprs137854535
ensemblrs137854535
gopubmedrs137854535
geneviewrs137854535
scholarrs137854535
googlers137854535
pharmgkbrs137854535
gwascentralrs137854535
openSNPrs137854535
23andMers137854535
23andMe allrs137854535
SNP Nexus

SNPshotrs137854535
SNPdbers137854535
MSV3drs137854535
GWAS Ctlgrs137854535
Max Magnitude0
OMIM139320
Desc
Variant0016
Relatedalso
ClinVar
Risk rs137854535(T;T)
Alt rs137854535(T;T)
Reference rs137854535(C;C)
Significance Pathogenic
Disease Pseudopseudohypoparathyroidism
Variation info
Gene GNAS
CLNDBN Pseudopseudohypoparathyroidism
Reversed 0
HGVS NC_000020.10:g.57484792C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017306.24,