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rs1064795725

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position53238140
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs1064795725
dbSNP (classic)rs1064795725
ClinGenrs1064795725
ebirs1064795725
HLIrs1064795725
Exacrs1064795725
Gnomadrs1064795725
Varsomers1064795725
LitVarrs1064795725
Maprs1064795725
PheGenIrs1064795725
Biobankrs1064795725
1000 genomesrs1064795725
hgdprs1064795725
ensemblrs1064795725
geneviewrs1064795725
scholarrs1064795725
googlers1064795725
pharmgkbrs1064795725
gwascentralrs1064795725
openSNPrs1064795725
23andMers1064795725
SNPshotrs1064795725
SNPdbers1064795725
MSV3drs1064795725
GWAS Ctlgrs1064795725
Max Magnitude0
ClinVar
Risk rs1064795725(A;A)
Alt rs1064795725(A;A)
Reference Rs1064795725(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IQSEC2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53267322C>T
CLNSRC
CLNACC RCV000487277.1,