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rs121908841

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908841(A;A)
Make rs121908841(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position189868615
GeneTP63
is asnp
is mentioned by
dbSNPrs121908841
ebirs121908841
HLIrs121908841
Exacrs121908841
Varsomers121908841
Maprs121908841
PheGenIrs121908841
hapmaprs121908841
1000 genomesrs121908841
hgdprs121908841
ensemblrs121908841
gopubmedrs121908841
geneviewrs121908841
scholarrs121908841
googlers121908841
pharmgkbrs121908841
gwascentralrs121908841
openSNPrs121908841
23andMers121908841
23andMe allrs121908841
SNP Nexus

SNPshotrs121908841
SNPdbers121908841
MSV3drs121908841
GWAS Ctlgrs121908841
Max Magnitude0
OMIM603273
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121908841(A;A)
Alt rs121908841(A;A)
Reference rs121908841(G;G)
Significance Pathogenic
Disease Ectrodactyly
Variation info
Gene TP63
CLNDBN Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3
Reversed 0
HGVS NC_000003.11:g.189586404G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006908.2,