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rs141019458

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs141019458(A;A)
Make rs141019458(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome17
Position39665425
GeneTCAP
is asnp
is mentioned by
dbSNPrs141019458
dbSNP (old)rs141019458
ClinGenrs141019458
ebirs141019458
HLIrs141019458
Exacrs141019458
Gnomadrs141019458
Varsomers141019458
LitVarrs141019458
Maprs141019458
PheGenIrs141019458
Biobankrs141019458
1000 genomesrs141019458
hgdprs141019458
ensemblrs141019458
gopubmedrs141019458
geneviewrs141019458
scholarrs141019458
googlers141019458
pharmgkbrs141019458
gwascentralrs141019458
openSNPrs141019458
23andMers141019458
23andMe allrs141019458
SNPshotrs141019458
SNPdbers141019458
MSV3drs141019458
GWAS Ctlgrs141019458
Max Magnitude0
ClinVar
Risk rs141019458(A;A)
Alt rs141019458(A;A)
Reference Rs141019458(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCAP
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.37821678G>A
CLNSRC
CLNACC RCV000400258.1,