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rs1064794702

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position5692911
GeneLINC01248, SOX11
is asnp
is mentioned by
dbSNPrs1064794702
dbSNP (old)rs1064794702
ClinGenrs1064794702
ebirs1064794702
HLIrs1064794702
Exacrs1064794702
Gnomadrs1064794702
Varsomers1064794702
Maprs1064794702
PheGenIrs1064794702
Biobankrs1064794702
1000 genomesrs1064794702
hgdprs1064794702
ensemblrs1064794702
gopubmedrs1064794702
geneviewrs1064794702
scholarrs1064794702
googlers1064794702
pharmgkbrs1064794702
gwascentralrs1064794702
openSNPrs1064794702
23andMers1064794702
23andMe allrs1064794702
SNPshotrs1064794702
SNPdbers1064794702
MSV3drs1064794702
GWAS Ctlgrs1064794702
Max Magnitude0
ClinVar
Risk rs1064794702(G;G)
Alt rs1064794702(G;G)
Reference Rs1064794702(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LINC01248 SOX11
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.5833043C>G
CLNSRC
CLNACC RCV000483495.1,