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rs886039388

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039388(C;T)
Make rs886039388(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position209796501
GeneIRF6
is asnp
is mentioned by
dbSNPrs886039388
dbSNP (classic)rs886039388
ClinGenrs886039388
ebirs886039388
HLIrs886039388
Exacrs886039388
Gnomadrs886039388
Varsomers886039388
LitVarrs886039388
Maprs886039388
PheGenIrs886039388
Biobankrs886039388
1000 genomesrs886039388
hgdprs886039388
ensemblrs886039388
geneviewrs886039388
scholarrs886039388
googlers886039388
pharmgkbrs886039388
gwascentralrs886039388
openSNPrs886039388
23andMers886039388
SNPshotrs886039388
SNPdbers886039388
MSV3drs886039388
GWAS Ctlgrs886039388
Max Magnitude0
ClinVar
Risk rs886039388(T;T)
Alt rs886039388(T;T)
Reference Rs886039388(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene IRF6
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.209969846G>A
CLNSRC
CLNACC RCV000255718.1,