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rs1057518399

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518399(A;A)
Make rs1057518399(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position189890818
GeneTP63
is asnp
is mentioned by
dbSNPrs1057518399
dbSNP (old)rs1057518399
ClinGenrs1057518399
ebirs1057518399
HLIrs1057518399
Exacrs1057518399
Gnomadrs1057518399
Varsomers1057518399
Maprs1057518399
PheGenIrs1057518399
Biobankrs1057518399
1000 genomesrs1057518399
hgdprs1057518399
ensemblrs1057518399
gopubmedrs1057518399
geneviewrs1057518399
scholarrs1057518399
googlers1057518399
pharmgkbrs1057518399
gwascentralrs1057518399
openSNPrs1057518399
23andMers1057518399
23andMe allrs1057518399
SNPshotrs1057518399
SNPdbers1057518399
MSV3drs1057518399
GWAS Ctlgrs1057518399
Max Magnitude0
ClinVar
Risk rs1057518399(A;A)
Alt rs1057518399(A;A)
Reference Rs1057518399(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TP63
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.189608607G>A
CLNSRC
CLNACC RCV000414275.1,