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rs104894943

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894943(C;T)
Make rs104894943(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position80026849
GeneTBX22
is asnp
is mentioned by
dbSNPrs104894943
ebirs104894943
HLIrs104894943
Exacrs104894943
Varsomers104894943
Maprs104894943
PheGenIrs104894943
hapmaprs104894943
1000 genomesrs104894943
hgdprs104894943
ensemblrs104894943
gopubmedrs104894943
geneviewrs104894943
scholarrs104894943
googlers104894943
pharmgkbrs104894943
gwascentralrs104894943
openSNPrs104894943
23andMers104894943
23andMe allrs104894943
SNP Nexus

SNPshotrs104894943
SNPdbers104894943
MSV3drs104894943
GWAS Ctlgrs104894943
Max Magnitude0
OMIM300307
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894943(T;T)
Alt rs104894943(T;T)
Reference rs104894943(C;C)
Significance Pathogenic
Disease Cleft palate with ankyloglossia
Variation info
Gene TBX22
CLNDBN Cleft palate with ankyloglossia
Reversed 0
HGVS NC_000023.10:g.79282348C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012082.3,