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rs1064795340

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome11
Position118491205
is asnp
is mentioned by
dbSNPrs1064795340
dbSNP (old)rs1064795340
ClinGenrs1064795340
ebirs1064795340
HLIrs1064795340
Exacrs1064795340
Gnomadrs1064795340
Varsomers1064795340
Maprs1064795340
PheGenIrs1064795340
Biobankrs1064795340
1000 genomesrs1064795340
hgdprs1064795340
ensemblrs1064795340
gopubmedrs1064795340
geneviewrs1064795340
scholarrs1064795340
googlers1064795340
pharmgkbrs1064795340
gwascentralrs1064795340
openSNPrs1064795340
23andMers1064795340
23andMe allrs1064795340
SNPshotrs1064795340
SNPdbers1064795340
MSV3drs1064795340
GWAS Ctlgrs1064795340
Max Magnitude0
ClinVar
Risk rs1064795340(TCTGAAACTC;TCTGAAACTC)
Alt rs1064795340(TCTGAAACTC;TCTGAAACTC)
Reference Rs1064795340(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118361920_118361921insAAACTCTCTG
CLNSRC
CLNACC RCV000482022.1,