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rs1057520098

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520098(G;T)
Make rs1057520098(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position30617488
GeneTCN2
is asnp
is mentioned by
dbSNPrs1057520098
dbSNP (old)rs1057520098
ClinGenrs1057520098
ebirs1057520098
HLIrs1057520098
Exacrs1057520098
Gnomadrs1057520098
Varsomers1057520098
LitVarrs1057520098
Maprs1057520098
PheGenIrs1057520098
Biobankrs1057520098
1000 genomesrs1057520098
hgdprs1057520098
ensemblrs1057520098
gopubmedrs1057520098
geneviewrs1057520098
scholarrs1057520098
googlers1057520098
pharmgkbrs1057520098
gwascentralrs1057520098
openSNPrs1057520098
23andMers1057520098
23andMe allrs1057520098
SNPshotrs1057520098
SNPdbers1057520098
MSV3drs1057520098
GWAS Ctlgrs1057520098
Max Magnitude0
ClinVar
Risk rs1057520098(T;T)
Alt rs1057520098(T;T)
Reference Rs1057520098(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCN2
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.31013475G>T
CLNSRC
CLNACC RCV000434122.1,