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rs1057520384

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520384(C;T)
Make rs1057520384(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position2166003
GeneTH
is asnp
is mentioned by
dbSNPrs1057520384
dbSNP (old)rs1057520384
ClinGenrs1057520384
ebirs1057520384
HLIrs1057520384
Exacrs1057520384
Gnomadrs1057520384
Varsomers1057520384
LitVarrs1057520384
Maprs1057520384
PheGenIrs1057520384
Biobankrs1057520384
1000 genomesrs1057520384
hgdprs1057520384
ensemblrs1057520384
gopubmedrs1057520384
geneviewrs1057520384
scholarrs1057520384
googlers1057520384
pharmgkbrs1057520384
gwascentralrs1057520384
openSNPrs1057520384
23andMers1057520384
23andMe allrs1057520384
SNPshotrs1057520384
SNPdbers1057520384
MSV3drs1057520384
GWAS Ctlgrs1057520384
Max Magnitude0
ClinVar
Risk rs1057520384(T;T)
Alt rs1057520384(T;T)
Reference Rs1057520384(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TH
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.2187233G>A
CLNSRC
CLNACC RCV000433260.1,