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rs1060499660

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499660(C;C)
Make rs1060499660(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position53248219
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs1060499660
dbSNP (old)rs1060499660
ClinGenrs1060499660
ebirs1060499660
HLIrs1060499660
Exacrs1060499660
Gnomadrs1060499660
Varsomers1060499660
Maprs1060499660
PheGenIrs1060499660
Biobankrs1060499660
1000 genomesrs1060499660
hgdprs1060499660
ensemblrs1060499660
gopubmedrs1060499660
geneviewrs1060499660
scholarrs1060499660
googlers1060499660
pharmgkbrs1060499660
gwascentralrs1060499660
openSNPrs1060499660
23andMers1060499660
23andMe allrs1060499660
SNPshotrs1060499660
SNPdbers1060499660
MSV3drs1060499660
GWAS Ctlgrs1060499660
Max Magnitude0
ClinVar
Risk rs1060499660(C;C)
Alt rs1060499660(C;C)
Reference Rs1060499660(T;T)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene IQSEC2
CLNDBN Mental retardation, X-linked 1
Reversed 1
HGVS NC_000023.10:g.53277401A>G
CLNSRC
CLNACC RCV000449548.1,