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rs121908849

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908849(A;A)
Make rs121908849(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position189866712
GeneTP63
is asnp
is mentioned by
dbSNPrs121908849
ebirs121908849
HLIrs121908849
Exacrs121908849
Varsomers121908849
Maprs121908849
PheGenIrs121908849
hapmaprs121908849
1000 genomesrs121908849
hgdprs121908849
ensemblrs121908849
gopubmedrs121908849
geneviewrs121908849
scholarrs121908849
googlers121908849
pharmgkbrs121908849
gwascentralrs121908849
openSNPrs121908849
23andMers121908849
23andMe allrs121908849
SNP Nexus

SNPshotrs121908849
SNPdbers121908849
MSV3drs121908849
GWAS Ctlgrs121908849
Max Magnitude0
OMIM603273
Desc
Variant0024
Relatedalso
ClinVar
Risk rs121908849(A;A)
Alt rs121908849(A;A)
Reference rs121908849(G;G)
Significance Pathogenic
Disease Ectrodactyly ADULT syndrome
Variation info
Gene TP63
CLNDBN Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 ADULT syndrome
Reversed 0
HGVS NC_000003.11:g.189584501G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006925.3, RCV000006926.3,