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rs879255245

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255245(C;T)
Make rs879255245(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position24342238
GeneGRHL3
is asnp
is mentioned by
dbSNPrs879255245
ebirs879255245
HLIrs879255245
Exacrs879255245
Varsomers879255245
Maprs879255245
PheGenIrs879255245
hapmaprs879255245
1000 genomesrs879255245
hgdprs879255245
ensemblrs879255245
gopubmedrs879255245
geneviewrs879255245
scholarrs879255245
googlers879255245
pharmgkbrs879255245
gwascentralrs879255245
openSNPrs879255245
23andMers879255245
23andMe allrs879255245
SNP Nexus

SNPshotrs879255245
SNPdbers879255245
MSV3drs879255245
GWAS Ctlgrs879255245
Max Magnitude0
ClinVar
Risk rs879255245(T;T)
Alt rs879255245(T;T)
Reference rs879255245(C;C)
Significance Pathogenic
Disease Van der Woude syndrome 2
Variation info
Gene GRHL3
CLNDBN Van der Woude syndrome 2
Reversed 0
HGVS NC_000001.10:g.24668728C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000087753.4,