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rs1057521750

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521750(C;C)
Make rs1057521750(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position189808464
GeneTP63
is asnp
is mentioned by
dbSNPrs1057521750
dbSNP (old)rs1057521750
ClinGenrs1057521750
ebirs1057521750
HLIrs1057521750
Exacrs1057521750
Gnomadrs1057521750
Varsomers1057521750
Maprs1057521750
PheGenIrs1057521750
Biobankrs1057521750
1000 genomesrs1057521750
hgdprs1057521750
ensemblrs1057521750
gopubmedrs1057521750
geneviewrs1057521750
scholarrs1057521750
googlers1057521750
pharmgkbrs1057521750
gwascentralrs1057521750
openSNPrs1057521750
23andMers1057521750
23andMe allrs1057521750
SNPshotrs1057521750
SNPdbers1057521750
MSV3drs1057521750
GWAS Ctlgrs1057521750
Max Magnitude0
ClinVar
Risk rs1057521750(C;C)
Alt rs1057521750(C;C)
Reference Rs1057521750(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TP63
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.189526253G>C
CLNSRC
CLNACC RCV000429171.1,