Have questions? Visit https://www.reddit.com/r/SNPedia

rs886039389

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039389(A;A)
Make rs886039389(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position209792360
GeneIRF6
is asnp
is mentioned by
dbSNPrs886039389
dbSNP (classic)rs886039389
ClinGenrs886039389
ebirs886039389
HLIrs886039389
Exacrs886039389
Gnomadrs886039389
Varsomers886039389
LitVarrs886039389
Maprs886039389
PheGenIrs886039389
Biobankrs886039389
1000 genomesrs886039389
hgdprs886039389
ensemblrs886039389
geneviewrs886039389
scholarrs886039389
googlers886039389
pharmgkbrs886039389
gwascentralrs886039389
openSNPrs886039389
23andMers886039389
SNPshotrs886039389
SNPdbers886039389
MSV3drs886039389
GWAS Ctlgrs886039389
Max Magnitude0
ClinVar
Risk rs886039389(A;A)
Alt rs886039389(A;A)
Reference Rs886039389(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene IRF6
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.209965705C>T
CLNSRC
CLNACC RCV000254805.1,