Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057520664

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520664(A;A)
Make rs1057520664(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position189867885
GeneTP63
is asnp
is mentioned by
dbSNPrs1057520664
dbSNP (old)rs1057520664
ClinGenrs1057520664
ebirs1057520664
HLIrs1057520664
Exacrs1057520664
Gnomadrs1057520664
Varsomers1057520664
Maprs1057520664
PheGenIrs1057520664
Biobankrs1057520664
1000 genomesrs1057520664
hgdprs1057520664
ensemblrs1057520664
gopubmedrs1057520664
geneviewrs1057520664
scholarrs1057520664
googlers1057520664
pharmgkbrs1057520664
gwascentralrs1057520664
openSNPrs1057520664
23andMers1057520664
23andMe allrs1057520664
SNPshotrs1057520664
SNPdbers1057520664
MSV3drs1057520664
GWAS Ctlgrs1057520664
Max Magnitude0
ClinVar
Risk rs1057520664(A;A)
Alt rs1057520664(A;A)
Reference Rs1057520664(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TP63
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.189585674G>A
CLNSRC
CLNACC RCV000435995.1,