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rs540215492

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs540215492(A;G)
Make rs540215492(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position21540529
GeneGYS2
is asnp
is mentioned by
dbSNPrs540215492
ebirs540215492
HLIrs540215492
Exacrs540215492
Varsomers540215492
Maprs540215492
PheGenIrs540215492
hapmaprs540215492
1000 genomesrs540215492
hgdprs540215492
ensemblrs540215492
gopubmedrs540215492
geneviewrs540215492
scholarrs540215492
googlers540215492
pharmgkbrs540215492
gwascentralrs540215492
openSNPrs540215492
23andMers540215492
23andMe allrs540215492
SNP Nexus

SNPshotrs540215492
SNPdbers540215492
MSV3drs540215492
GWAS Ctlgrs540215492
Max Magnitude0
ClinVar
Risk rs540215492(G;G)
Alt rs540215492(G;G)
Reference rs540215492(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GYS2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.21693463A>G
CLNSRC
CLNACC RCV000198163.1,