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rs1064795728

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAACT;GAACT) 0 common in clinvar
Chromosome1
Position99921558
GeneAGL
is asnp
is mentioned by
dbSNPrs1064795728
dbSNP (classic)rs1064795728
ClinGenrs1064795728
ebirs1064795728
HLIrs1064795728
Exacrs1064795728
Gnomadrs1064795728
Varsomers1064795728
LitVarrs1064795728
Maprs1064795728
PheGenIrs1064795728
Biobankrs1064795728
1000 genomesrs1064795728
hgdprs1064795728
ensemblrs1064795728
geneviewrs1064795728
scholarrs1064795728
googlers1064795728
pharmgkbrs1064795728
gwascentralrs1064795728
openSNPrs1064795728
23andMers1064795728
SNPshotrs1064795728
SNPdbers1064795728
MSV3drs1064795728
GWAS Ctlgrs1064795728
Max Magnitude0
ClinVar
Risk rs1064795728(-;-)
Alt rs1064795728(-;-)
Reference Rs1064795728(GAACT;GAACT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AGL
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.100387114_100387118delACTGA
CLNSRC
CLNACC RCV000482459.1,