Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1064793681

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GACATTG;GACATTG) 0 common in clinvar
Chromosome6
Position85507265
GeneSNX14
is asnp
is mentioned by
dbSNPrs1064793681
dbSNP (old)rs1064793681
ClinGenrs1064793681
ebirs1064793681
HLIrs1064793681
Exacrs1064793681
Gnomadrs1064793681
Varsomers1064793681
Maprs1064793681
PheGenIrs1064793681
Biobankrs1064793681
1000 genomesrs1064793681
hgdprs1064793681
ensemblrs1064793681
gopubmedrs1064793681
geneviewrs1064793681
scholarrs1064793681
googlers1064793681
pharmgkbrs1064793681
gwascentralrs1064793681
openSNPrs1064793681
23andMers1064793681
23andMe allrs1064793681
SNPshotrs1064793681
SNPdbers1064793681
MSV3drs1064793681
GWAS Ctlgrs1064793681
Max Magnitude0
ClinVar
Risk rs1064793681(-;-)
Alt rs1064793681(-;-)
Reference Rs1064793681(GACATTG;GACATTG)
Significance Pathogenic
Disease not provided
Variation info
Gene SNX14
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.86216983_86216989delCAATGTC
CLNSRC
CLNACC RCV000485240.1,