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rs1060499555

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499555(C;C)
Make rs1060499555(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position209801301
GeneIRF6
is asnp
is mentioned by
dbSNPrs1060499555
dbSNP (old)rs1060499555
ClinGenrs1060499555
ebirs1060499555
HLIrs1060499555
Exacrs1060499555
Gnomadrs1060499555
Varsomers1060499555
Maprs1060499555
PheGenIrs1060499555
Biobankrs1060499555
1000 genomesrs1060499555
hgdprs1060499555
ensemblrs1060499555
gopubmedrs1060499555
geneviewrs1060499555
scholarrs1060499555
googlers1060499555
pharmgkbrs1060499555
gwascentralrs1060499555
openSNPrs1060499555
23andMers1060499555
23andMe allrs1060499555
SNPshotrs1060499555
SNPdbers1060499555
MSV3drs1060499555
GWAS Ctlgrs1060499555
Max Magnitude0
ClinVar
Risk rs1060499555(C;C)
Alt rs1060499555(C;C)
Reference Rs1060499555(T;T)
Significance Pathogenic
Disease Van der Woude syndrome
Variation info
Gene IRF6
CLNDBN Van der Woude syndrome
Reversed 1
HGVS NC_000001.10:g.209974646A>G
CLNSRC
CLNACC RCV000449637.1,