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rs1085307630

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position53236500
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs1085307630
dbSNP (old)rs1085307630
ClinGenrs1085307630
ebirs1085307630
HLIrs1085307630
Exacrs1085307630
Gnomadrs1085307630
Varsomers1085307630
Maprs1085307630
PheGenIrs1085307630
Biobankrs1085307630
1000 genomesrs1085307630
hgdprs1085307630
ensemblrs1085307630
gopubmedrs1085307630
geneviewrs1085307630
scholarrs1085307630
googlers1085307630
pharmgkbrs1085307630
gwascentralrs1085307630
openSNPrs1085307630
23andMers1085307630
23andMe allrs1085307630
SNPshotrs1085307630
SNPdbers1085307630
MSV3drs1085307630
GWAS Ctlgrs1085307630
Max Magnitude0
ClinVar
Risk rs1085307630(G;G)
Alt rs1085307630(G;G)
Reference Rs1085307630(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IQSEC2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53265682G>C
CLNSRC
CLNACC RCV000489196.1,