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rs1064794911

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome9
Position136197647
GeneLHX3
is asnp
is mentioned by
dbSNPrs1064794911
dbSNP (old)rs1064794911
ClinGenrs1064794911
ebirs1064794911
HLIrs1064794911
Exacrs1064794911
Gnomadrs1064794911
Varsomers1064794911
Maprs1064794911
PheGenIrs1064794911
Biobankrs1064794911
1000 genomesrs1064794911
hgdprs1064794911
ensemblrs1064794911
gopubmedrs1064794911
geneviewrs1064794911
scholarrs1064794911
googlers1064794911
pharmgkbrs1064794911
gwascentralrs1064794911
openSNPrs1064794911
23andMers1064794911
23andMe allrs1064794911
SNPshotrs1064794911
SNPdbers1064794911
MSV3drs1064794911
GWAS Ctlgrs1064794911
Max Magnitude0
ClinVar
Risk rs1064794911(-;-)
Alt rs1064794911(-;-)
Reference Rs1064794911(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LHX3
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.139089493delC
CLNSRC
CLNACC RCV000484284.1,