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rs886039570

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039570(G;T)
Make rs886039570(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position209801260
GeneIRF6
is asnp
is mentioned by
dbSNPrs886039570
dbSNP (classic)rs886039570
ClinGenrs886039570
ebirs886039570
HLIrs886039570
Exacrs886039570
Gnomadrs886039570
Varsomers886039570
LitVarrs886039570
Maprs886039570
PheGenIrs886039570
Biobankrs886039570
1000 genomesrs886039570
hgdprs886039570
ensemblrs886039570
geneviewrs886039570
scholarrs886039570
googlers886039570
pharmgkbrs886039570
gwascentralrs886039570
openSNPrs886039570
23andMers886039570
SNPshotrs886039570
SNPdbers886039570
MSV3drs886039570
GWAS Ctlgrs886039570
Max Magnitude0
ClinVar
Risk rs886039570(T;T)
Alt rs886039570(T;T)
Reference Rs886039570(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene IRF6
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.209974605C>A
CLNSRC
CLNACC RCV000255193.1,