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rs1057524157

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524157(G;G)
Make rs1057524157(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position686962
GeneDEAF1
is asnp
is mentioned by
dbSNPrs1057524157
dbSNP (old)rs1057524157
ClinGenrs1057524157
ebirs1057524157
HLIrs1057524157
Exacrs1057524157
Gnomadrs1057524157
Varsomers1057524157
Maprs1057524157
PheGenIrs1057524157
Biobankrs1057524157
1000 genomesrs1057524157
hgdprs1057524157
ensemblrs1057524157
gopubmedrs1057524157
geneviewrs1057524157
scholarrs1057524157
googlers1057524157
pharmgkbrs1057524157
gwascentralrs1057524157
openSNPrs1057524157
23andMers1057524157
23andMe allrs1057524157
SNPshotrs1057524157
SNPdbers1057524157
MSV3drs1057524157
GWAS Ctlgrs1057524157
Max Magnitude0
ClinVar
Risk rs1057524157(G;G)
Alt rs1057524157(G;G)
Reference Rs1057524157(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DEAF1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.686962A>C
CLNSRC
CLNACC RCV000443903.1,