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

rs1085307451

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome3
Position47848246
GeneDHX30, MIR1226
is asnp
is mentioned by
dbSNPrs1085307451
dbSNP (old)rs1085307451
ClinGenrs1085307451
ebirs1085307451
HLIrs1085307451
Exacrs1085307451
Gnomadrs1085307451
Varsomers1085307451
Maprs1085307451
PheGenIrs1085307451
Biobankrs1085307451
1000 genomesrs1085307451
hgdprs1085307451
ensemblrs1085307451
gopubmedrs1085307451
geneviewrs1085307451
scholarrs1085307451
googlers1085307451
pharmgkbrs1085307451
gwascentralrs1085307451
openSNPrs1085307451
23andMers1085307451
23andMe allrs1085307451
SNPshotrs1085307451
SNPdbers1085307451
MSV3drs1085307451
GWAS Ctlgrs1085307451
Max Magnitude0
ClinVar
Risk rs1085307451(T;T)
Alt rs1085307451(T;T)
Reference Rs1085307451(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR1226 DHX30
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.47889736C>T
CLNSRC
CLNACC RCV000489269.1,