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

rs1064793267

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome5
Position149031551
GeneSH3TC2
is asnp
is mentioned by
dbSNPrs1064793267
dbSNP (old)rs1064793267
ClinGenrs1064793267
ebirs1064793267
HLIrs1064793267
Exacrs1064793267
Gnomadrs1064793267
Varsomers1064793267
Maprs1064793267
PheGenIrs1064793267
Biobankrs1064793267
1000 genomesrs1064793267
hgdprs1064793267
ensemblrs1064793267
gopubmedrs1064793267
geneviewrs1064793267
scholarrs1064793267
googlers1064793267
pharmgkbrs1064793267
gwascentralrs1064793267
openSNPrs1064793267
23andMers1064793267
23andMe allrs1064793267
SNPshotrs1064793267
SNPdbers1064793267
MSV3drs1064793267
GWAS Ctlgrs1064793267
Max Magnitude0
ClinVar
Risk rs1064793267(C;C)
Alt rs1064793267(C;C)
Reference Rs1064793267(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SH3TC2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.148411114C>G
CLNSRC
CLNACC RCV000480598.1,