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rs1064795630

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTTCTA;CTTCTA) 0 common in clinvar
Chromosome1
Position99891633
GeneAGL
is asnp
is mentioned by
dbSNPrs1064795630
dbSNP (old)rs1064795630
ClinGenrs1064795630
ebirs1064795630
HLIrs1064795630
Exacrs1064795630
Gnomadrs1064795630
Varsomers1064795630
Maprs1064795630
PheGenIrs1064795630
Biobankrs1064795630
1000 genomesrs1064795630
hgdprs1064795630
ensemblrs1064795630
gopubmedrs1064795630
geneviewrs1064795630
scholarrs1064795630
googlers1064795630
pharmgkbrs1064795630
gwascentralrs1064795630
openSNPrs1064795630
23andMers1064795630
23andMe allrs1064795630
SNPshotrs1064795630
SNPdbers1064795630
MSV3drs1064795630
GWAS Ctlgrs1064795630
Max Magnitude0
ClinVar
Risk rs1064795630(-;-)
Alt rs1064795630(-;-)
Reference Rs1064795630(CTTCTA;CTTCTA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AGL
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.100357189_100357194delTTCTAC
CLNSRC
CLNACC RCV000482990.1,