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rs28942095

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28942095(C;T)
Make rs28942095(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position209788626
GeneIRF6
is asnp
is mentioned by
dbSNPrs28942095
ebirs28942095
HLIrs28942095
Exacrs28942095
Varsomers28942095
Maprs28942095
PheGenIrs28942095
hapmaprs28942095
1000 genomesrs28942095
hgdprs28942095
ensemblrs28942095
gopubmedrs28942095
geneviewrs28942095
scholarrs28942095
googlers28942095
pharmgkbrs28942095
gwascentralrs28942095
openSNPrs28942095
23andMers28942095
23andMe allrs28942095
SNP Nexus

SNPshotrs28942095
SNPdbers28942095
MSV3drs28942095
GWAS Ctlgrs28942095
Max Magnitude0
OMIM607199
DescVAN DER WOUDE SYNDROME
Variant0009
Relatedalso
ClinVar
Risk rs28942095(T;T)
Alt rs28942095(T;T)
Reference rs28942095(C;C)
Significance Pathogenic
Disease Van der Woude syndrome
Variation info
Gene IRF6
CLNDBN Van der Woude syndrome
Reversed 1
HGVS NC_000001.10:g.209961971G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003588.5,