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rs121908835

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908835(C;T)
Make rs121908835(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position189864379
GeneTP63
is asnp
is mentioned by
dbSNPrs121908835
ebirs121908835
HLIrs121908835
Exacrs121908835
Varsomers121908835
Maprs121908835
PheGenIrs121908835
hapmaprs121908835
1000 genomesrs121908835
hgdprs121908835
ensemblrs121908835
gopubmedrs121908835
geneviewrs121908835
scholarrs121908835
googlers121908835
pharmgkbrs121908835
gwascentralrs121908835
openSNPrs121908835
23andMers121908835
23andMe allrs121908835
SNP Nexus

SNPshotrs121908835
SNPdbers121908835
MSV3drs121908835
GWAS Ctlgrs121908835
Max Magnitude0
OMIM603273
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908835(T;T)
Alt rs121908835(T;T)
Reference rs121908835(C;C)
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.189582168C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006900.5,