Have questions? Visit https://www.reddit.com/r/SNPedia

rs121908844

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908844(A;G)
Make rs121908844(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position189868639
GeneTP63
is asnp
is mentioned by
dbSNPrs121908844
dbSNP (classic)rs121908844
ClinGenrs121908844
ebirs121908844
HLIrs121908844
Exacrs121908844
Gnomadrs121908844
Varsomers121908844
LitVarrs121908844
Maprs121908844
PheGenIrs121908844
Biobankrs121908844
1000 genomesrs121908844
hgdprs121908844
ensemblrs121908844
geneviewrs121908844
scholarrs121908844
googlers121908844
pharmgkbrs121908844
gwascentralrs121908844
openSNPrs121908844
23andMers121908844
SNPshotrs121908844
SNPdbers121908844
MSV3drs121908844
GWAS Ctlgrs121908844
Max Magnitude0
OMIM603273
Desc
Variant0015
Relatedalso
ClinVar
Risk rs121908844(G;G)
Alt rs121908844(G;G)
Reference Rs121908844(A;A)
Significance Pathogenic
Disease Ectrodactyly not provided
Variation info
Gene TP63
CLNDBN Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 not provided
Reversed 0
HGVS NC_000003.11:g.189586428A>G
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000006915.2, RCV000326964.1,