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rs1064796510

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome1
Position47260541
GeneSTIL
is asnp
is mentioned by
dbSNPrs1064796510
dbSNP (old)rs1064796510
ClinGenrs1064796510
ebirs1064796510
HLIrs1064796510
Exacrs1064796510
Gnomadrs1064796510
Varsomers1064796510
Maprs1064796510
PheGenIrs1064796510
Biobankrs1064796510
1000 genomesrs1064796510
hgdprs1064796510
ensemblrs1064796510
gopubmedrs1064796510
geneviewrs1064796510
scholarrs1064796510
googlers1064796510
pharmgkbrs1064796510
gwascentralrs1064796510
openSNPrs1064796510
23andMers1064796510
23andMe allrs1064796510
SNPshotrs1064796510
SNPdbers1064796510
MSV3drs1064796510
GWAS Ctlgrs1064796510
Max Magnitude0
ClinVar
Risk rs1064796510(G;G)
Alt rs1064796510(G;G)
Reference Rs1064796510(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene STIL
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.47726213T>C
CLNSRC
CLNACC RCV000484930.1,