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rs1057520858

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520858(C;T)
Make rs1057520858(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position53243445
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs1057520858
dbSNP (old)rs1057520858
ClinGenrs1057520858
ebirs1057520858
HLIrs1057520858
Exacrs1057520858
Gnomadrs1057520858
Varsomers1057520858
LitVarrs1057520858
Maprs1057520858
PheGenIrs1057520858
Biobankrs1057520858
1000 genomesrs1057520858
hgdprs1057520858
ensemblrs1057520858
gopubmedrs1057520858
geneviewrs1057520858
scholarrs1057520858
googlers1057520858
pharmgkbrs1057520858
gwascentralrs1057520858
openSNPrs1057520858
23andMers1057520858
23andMe allrs1057520858
SNPshotrs1057520858
SNPdbers1057520858
MSV3drs1057520858
GWAS Ctlgrs1057520858
Max Magnitude0
ClinVar
Risk rs1057520858(T;T)
Alt rs1057520858(T;T)
Reference Rs1057520858(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene IQSEC2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53272627G>A
CLNSRC
CLNACC RCV000422126.1,