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rs1057521657

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521657(C;T)
Make rs1057521657(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position53241816
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs1057521657
dbSNP (old)rs1057521657
ClinGenrs1057521657
ebirs1057521657
HLIrs1057521657
Exacrs1057521657
Gnomadrs1057521657
Varsomers1057521657
Maprs1057521657
PheGenIrs1057521657
Biobankrs1057521657
1000 genomesrs1057521657
hgdprs1057521657
ensemblrs1057521657
gopubmedrs1057521657
geneviewrs1057521657
scholarrs1057521657
googlers1057521657
pharmgkbrs1057521657
gwascentralrs1057521657
openSNPrs1057521657
23andMers1057521657
23andMe allrs1057521657
SNPshotrs1057521657
SNPdbers1057521657
MSV3drs1057521657
GWAS Ctlgrs1057521657
Max Magnitude0
ClinVar
Risk rs1057521657(T;T)
Alt rs1057521657(T;T)
Reference Rs1057521657(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IQSEC2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53270998G>A
CLNSRC
CLNACC RCV000425290.1,