rs111541229

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs111541229(C;C)

Make rs111541229(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

58898986

Gene

GNAS

is a	snp
is	mentioned by
dbSNP	rs111541229
dbSNP (classic)	rs111541229
ClinGen	rs111541229
ebi	rs111541229
HLI	rs111541229
Exac	rs111541229
Gnomad	rs111541229
Varsome	rs111541229
LitVar	rs111541229
Map	rs111541229
PheGenI	rs111541229
Biobank	rs111541229
1000 genomes	rs111541229
hgdp	rs111541229
ensembl	rs111541229
geneview	rs111541229
scholar	rs111541229
google	rs111541229
pharmgkb	rs111541229
gwascentral	rs111541229
openSNP	rs111541229
23andMe	rs111541229
SNPshot	rs111541229
SNPdbe	rs111541229
MSV3d	rs111541229
GWAS Ctlg	rs111541229

Max Magnitude

0

ClinVar
Risk	rs111541229(C;C) rs111541229(T;T)
Alt	rs111541229(C;C) rs111541229(T;T)
Reference	Rs111541229(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GNAS
CLNDBN	not provided
Reversed	0
HGVS	NC_000020.10:g.57474041G>T
CLNSRC
CLNACC	RCV000482442.1,