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rs121908839

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908839(C;T)
Make rs121908839(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position189867905
GeneTP63
is asnp
is mentioned by
dbSNPrs121908839
ebirs121908839
HLIrs121908839
Exacrs121908839
Varsomers121908839
Maprs121908839
PheGenIrs121908839
hapmaprs121908839
1000 genomesrs121908839
hgdprs121908839
ensemblrs121908839
gopubmedrs121908839
geneviewrs121908839
scholarrs121908839
googlers121908839
pharmgkbrs121908839
gwascentralrs121908839
openSNPrs121908839
23andMers121908839
23andMe allrs121908839
SNP Nexus

SNPshotrs121908839
SNPdbers121908839
MSV3drs121908839
GWAS Ctlgrs121908839
Max Magnitude0
OMIM603273
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121908839(T;T)
Alt rs121908839(T;T)
Reference rs121908839(C;C)
Significance Pathogenic
Disease Split-hand/foot malformation 4
Variation info
Gene TP63
CLNDBN Split-hand/foot malformation 4
Reversed 0
HGVS NC_000003.11:g.189585694C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006905.2,