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rs1057520738

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520738(C;T)
Make rs1057520738(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position209795344
GeneIRF6
is asnp
is mentioned by
dbSNPrs1057520738
dbSNP (old)rs1057520738
ClinGenrs1057520738
ebirs1057520738
HLIrs1057520738
Exacrs1057520738
Gnomadrs1057520738
Varsomers1057520738
LitVarrs1057520738
Maprs1057520738
PheGenIrs1057520738
Biobankrs1057520738
1000 genomesrs1057520738
hgdprs1057520738
ensemblrs1057520738
gopubmedrs1057520738
geneviewrs1057520738
scholarrs1057520738
googlers1057520738
pharmgkbrs1057520738
gwascentralrs1057520738
openSNPrs1057520738
23andMers1057520738
23andMe allrs1057520738
SNPshotrs1057520738
SNPdbers1057520738
MSV3drs1057520738
GWAS Ctlgrs1057520738
Max Magnitude0
ClinVar
Risk rs1057520738(T;T)
Alt rs1057520738(T;T)
Reference Rs1057520738(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene IRF6
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.209968689G>A
CLNSRC
CLNACC RCV000443013.1,