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rs1064794955

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position190989659
GeneSTAT1
is asnp
is mentioned by
dbSNPrs1064794955
dbSNP (classic)rs1064794955
ClinGenrs1064794955
ebirs1064794955
HLIrs1064794955
Exacrs1064794955
Gnomadrs1064794955
Varsomers1064794955
LitVarrs1064794955
Maprs1064794955
PheGenIrs1064794955
Biobankrs1064794955
1000 genomesrs1064794955
hgdprs1064794955
ensemblrs1064794955
geneviewrs1064794955
scholarrs1064794955
googlers1064794955
pharmgkbrs1064794955
gwascentralrs1064794955
openSNPrs1064794955
23andMers1064794955
23andMe allrs1064794955
SNPshotrs1064794955
SNPdbers1064794955
MSV3drs1064794955
GWAS Ctlgrs1064794955
Max Magnitude0
ClinVar
Risk rs1064794955(T;T)
Alt rs1064794955(T;T)
Reference Rs1064794955(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STAT1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.191854385C>A
CLNSRC
CLNACC RCV000480463.1,