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

rs1057520174

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520174(A;A)
Make rs1057520174(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position110263959
GeneRDX
is asnp
is mentioned by
dbSNPrs1057520174
dbSNP (old)rs1057520174
ClinGenrs1057520174
ebirs1057520174
HLIrs1057520174
Exacrs1057520174
Gnomadrs1057520174
Varsomers1057520174
Maprs1057520174
PheGenIrs1057520174
Biobankrs1057520174
1000 genomesrs1057520174
hgdprs1057520174
ensemblrs1057520174
gopubmedrs1057520174
geneviewrs1057520174
scholarrs1057520174
googlers1057520174
pharmgkbrs1057520174
gwascentralrs1057520174
openSNPrs1057520174
23andMers1057520174
23andMe allrs1057520174
SNPshotrs1057520174
SNPdbers1057520174
MSV3drs1057520174
GWAS Ctlgrs1057520174
Max Magnitude0
ClinVar
Risk rs1057520174(A;A)
Alt rs1057520174(A;A)
Reference Rs1057520174(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RDX
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.110134684C>T
CLNSRC
CLNACC RCV000429322.1,