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rs1057519220

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519220(C;T)
Make rs1057519220(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position2169670
GeneTH
is asnp
is mentioned by
dbSNPrs1057519220
dbSNP (old)rs1057519220
ClinGenrs1057519220
ebirs1057519220
HLIrs1057519220
Exacrs1057519220
Gnomadrs1057519220
Varsomers1057519220
Maprs1057519220
PheGenIrs1057519220
Biobankrs1057519220
1000 genomesrs1057519220
hgdprs1057519220
ensemblrs1057519220
gopubmedrs1057519220
geneviewrs1057519220
scholarrs1057519220
googlers1057519220
pharmgkbrs1057519220
gwascentralrs1057519220
openSNPrs1057519220
23andMers1057519220
23andMe allrs1057519220
SNPshotrs1057519220
SNPdbers1057519220
MSV3drs1057519220
GWAS Ctlgrs1057519220
Max Magnitude0
ClinVar
Risk rs1057519220(T;T)
Alt rs1057519220(T;T)
Reference Rs1057519220(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TH
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.2190900G>A
CLNSRC
CLNACC RCV000415910.2,