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rs863224039

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224039(A;A)
Make rs863224039(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position21546466
GeneGYS2
is asnp
is mentioned by
dbSNPrs863224039
ebirs863224039
HLIrs863224039
Exacrs863224039
Varsomers863224039
Maprs863224039
PheGenIrs863224039
hapmaprs863224039
1000 genomesrs863224039
hgdprs863224039
ensemblrs863224039
gopubmedrs863224039
geneviewrs863224039
scholarrs863224039
googlers863224039
pharmgkbrs863224039
gwascentralrs863224039
openSNPrs863224039
23andMers863224039
23andMe allrs863224039
SNP Nexus

SNPshotrs863224039
SNPdbers863224039
MSV3drs863224039
GWAS Ctlgrs863224039
Max Magnitude0
ClinVar
Risk rs863224039(A;A)
Alt rs863224039(A;A)
Reference rs863224039(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GYS2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.21699400A>T
CLNSRC
CLNACC RCV000199996.1,