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rs1057520382

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520382(A;A)
Make rs1057520382(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position20043375
GeneTANGO2
is asnp
is mentioned by
dbSNPrs1057520382
dbSNP (classic)rs1057520382
ClinGenrs1057520382
ebirs1057520382
HLIrs1057520382
Exacrs1057520382
Gnomadrs1057520382
Varsomers1057520382
LitVarrs1057520382
Maprs1057520382
PheGenIrs1057520382
Biobankrs1057520382
1000 genomesrs1057520382
hgdprs1057520382
ensemblrs1057520382
geneviewrs1057520382
scholarrs1057520382
googlers1057520382
pharmgkbrs1057520382
gwascentralrs1057520382
openSNPrs1057520382
23andMers1057520382
23andMe allrs1057520382
SNPshotrs1057520382
SNPdbers1057520382
MSV3drs1057520382
GWAS Ctlgrs1057520382
Max Magnitude0
ClinVar
Risk rs1057520382(A;A)
Alt rs1057520382(A;A)
Reference Rs1057520382(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TANGO2
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.20030898G>A
CLNSRC
CLNACC RCV000424981.1,