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rs1064795983

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome1
Position152304695
GeneFLG
is asnp
is mentioned by
dbSNPrs1064795983
dbSNP (old)rs1064795983
ClinGenrs1064795983
ebirs1064795983
HLIrs1064795983
Exacrs1064795983
Gnomadrs1064795983
Varsomers1064795983
Maprs1064795983
PheGenIrs1064795983
Biobankrs1064795983
1000 genomesrs1064795983
hgdprs1064795983
ensemblrs1064795983
gopubmedrs1064795983
geneviewrs1064795983
scholarrs1064795983
googlers1064795983
pharmgkbrs1064795983
gwascentralrs1064795983
openSNPrs1064795983
23andMers1064795983
23andMe allrs1064795983
SNPshotrs1064795983
SNPdbers1064795983
MSV3drs1064795983
GWAS Ctlgrs1064795983
Max Magnitude0
ClinVar
Risk rs1064795983(-;-)
Alt rs1064795983(-;-)
Reference Rs1064795983(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.152277171delC
CLNSRC
CLNACC RCV000478664.1,