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rs1057517985

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517985(A;G)
Make rs1057517985(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position189868635
GeneTP63
is asnp
is mentioned by
dbSNPrs1057517985
dbSNP (old)rs1057517985
ClinGenrs1057517985
ebirs1057517985
HLIrs1057517985
Exacrs1057517985
Gnomadrs1057517985
Varsomers1057517985
LitVarrs1057517985
Maprs1057517985
PheGenIrs1057517985
Biobankrs1057517985
1000 genomesrs1057517985
hgdprs1057517985
ensemblrs1057517985
gopubmedrs1057517985
geneviewrs1057517985
scholarrs1057517985
googlers1057517985
pharmgkbrs1057517985
gwascentralrs1057517985
openSNPrs1057517985
23andMers1057517985
23andMe allrs1057517985
SNPshotrs1057517985
SNPdbers1057517985
MSV3drs1057517985
GWAS Ctlgrs1057517985
Max Magnitude0
ClinVar
Risk rs1057517985(G;G)
Alt rs1057517985(G;G)
Reference Rs1057517985(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TP63
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.189586424A>G
CLNSRC
CLNACC RCV000413411.1,