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rs1064796105

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome1
Position152305164
GeneFLG
is asnp
is mentioned by
dbSNPrs1064796105
dbSNP (old)rs1064796105
ClinGenrs1064796105
ebirs1064796105
HLIrs1064796105
Exacrs1064796105
Gnomadrs1064796105
Varsomers1064796105
LitVarrs1064796105
Maprs1064796105
PheGenIrs1064796105
Biobankrs1064796105
1000 genomesrs1064796105
hgdprs1064796105
ensemblrs1064796105
gopubmedrs1064796105
geneviewrs1064796105
scholarrs1064796105
googlers1064796105
pharmgkbrs1064796105
gwascentralrs1064796105
openSNPrs1064796105
23andMers1064796105
23andMe allrs1064796105
SNPshotrs1064796105
SNPdbers1064796105
MSV3drs1064796105
GWAS Ctlgrs1064796105
Max Magnitude0
ClinVar
Risk rs1064796105(-;-)
Alt rs1064796105(-;-)
Reference Rs1064796105(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.152277640delC
CLNSRC
CLNACC RCV000484399.1,