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rs201157731

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201157731(A;A)
Make rs201157731(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position21574275
GeneGYS2
is asnp
is mentioned by
dbSNPrs201157731
ebirs201157731
HLIrs201157731
Exacrs201157731
Varsomers201157731
Maprs201157731
PheGenIrs201157731
hapmaprs201157731
1000 genomesrs201157731
hgdprs201157731
ensemblrs201157731
gopubmedrs201157731
geneviewrs201157731
scholarrs201157731
googlers201157731
pharmgkbrs201157731
gwascentralrs201157731
openSNPrs201157731
23andMers201157731
23andMe allrs201157731
SNP Nexus

SNPshotrs201157731
SNPdbers201157731
MSV3drs201157731
GWAS Ctlgrs201157731
Max Magnitude0
ClinVar
Risk rs201157731(A;A)
Alt rs201157731(A;A)
Reference rs201157731(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GYS2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.21727209G>A
CLNSRC
CLNACC RCV000199810.1,