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

rs150382575

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150382575(A;A)
Make rs150382575(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position21574248
GeneGYS2
is asnp
is mentioned by
dbSNPrs150382575
ebirs150382575
HLIrs150382575
Exacrs150382575
Varsomers150382575
Maprs150382575
PheGenIrs150382575
hapmaprs150382575
1000 genomesrs150382575
hgdprs150382575
ensemblrs150382575
gopubmedrs150382575
geneviewrs150382575
scholarrs150382575
googlers150382575
pharmgkbrs150382575
gwascentralrs150382575
openSNPrs150382575
23andMers150382575
23andMe allrs150382575
SNP Nexus

SNPshotrs150382575
SNPdbers150382575
MSV3drs150382575
GWAS Ctlgrs150382575
Max Magnitude0
ClinVar
Risk rs150382575(A,T;A,T)
Alt rs150382575(A,T;A,T)
Reference rs150382575(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GYS2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.21727182G>A
CLNSRC
CLNACC RCV000196241.1,