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rs1064796614

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position53238172
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs1064796614
dbSNP (classic)rs1064796614
ClinGenrs1064796614
ebirs1064796614
HLIrs1064796614
Exacrs1064796614
Gnomadrs1064796614
Varsomers1064796614
LitVarrs1064796614
Maprs1064796614
PheGenIrs1064796614
Biobankrs1064796614
1000 genomesrs1064796614
hgdprs1064796614
ensemblrs1064796614
geneviewrs1064796614
scholarrs1064796614
googlers1064796614
pharmgkbrs1064796614
gwascentralrs1064796614
openSNPrs1064796614
23andMers1064796614
23andMe allrs1064796614
SNPshotrs1064796614
SNPdbers1064796614
MSV3drs1064796614
GWAS Ctlgrs1064796614
Max Magnitude0
ClinVar
Risk rs1064796614(T;T)
Alt rs1064796614(T;T)
Reference Rs1064796614(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene IQSEC2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53267354G>A
CLNSRC
CLNACC RCV000484641.1,