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rs1064793143

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome12
Position21546371
GeneGYS2
is asnp
is mentioned by
dbSNPrs1064793143
dbSNP (old)rs1064793143
ClinGenrs1064793143
ebirs1064793143
HLIrs1064793143
Exacrs1064793143
Gnomadrs1064793143
Varsomers1064793143
LitVarrs1064793143
Maprs1064793143
PheGenIrs1064793143
Biobankrs1064793143
1000 genomesrs1064793143
hgdprs1064793143
ensemblrs1064793143
gopubmedrs1064793143
geneviewrs1064793143
scholarrs1064793143
googlers1064793143
pharmgkbrs1064793143
gwascentralrs1064793143
openSNPrs1064793143
23andMers1064793143
23andMe allrs1064793143
SNPshotrs1064793143
SNPdbers1064793143
MSV3drs1064793143
GWAS Ctlgrs1064793143
Max Magnitude0
ClinVar
Risk rs1064793143(G;G)
Alt rs1064793143(G;G)
Reference Rs1064793143(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GYS2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.21699305A>C
CLNSRC
CLNACC RCV000482018.1,