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rs1057521133

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521133(A;G)
Make rs1057521133(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position209801314
GeneIRF6
is asnp
is mentioned by
dbSNPrs1057521133
dbSNP (old)rs1057521133
ClinGenrs1057521133
ebirs1057521133
HLIrs1057521133
Exacrs1057521133
Gnomadrs1057521133
Varsomers1057521133
Maprs1057521133
PheGenIrs1057521133
Biobankrs1057521133
1000 genomesrs1057521133
hgdprs1057521133
ensemblrs1057521133
gopubmedrs1057521133
geneviewrs1057521133
scholarrs1057521133
googlers1057521133
pharmgkbrs1057521133
gwascentralrs1057521133
openSNPrs1057521133
23andMers1057521133
23andMe allrs1057521133
SNPshotrs1057521133
SNPdbers1057521133
MSV3drs1057521133
GWAS Ctlgrs1057521133
Max Magnitude0
ClinVar
Risk rs1057521133(G;G)
Alt rs1057521133(G;G)
Reference Rs1057521133(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IRF6
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.209974659T>C
CLNSRC
CLNACC RCV000437849.1,