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

rs1057521725

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521725(A;A)
Make rs1057521725(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position7579859
GeneRBFOX1
is asnp
is mentioned by
dbSNPrs1057521725
dbSNP (old)rs1057521725
ClinGenrs1057521725
ebirs1057521725
HLIrs1057521725
Exacrs1057521725
Gnomadrs1057521725
Varsomers1057521725
Maprs1057521725
PheGenIrs1057521725
Biobankrs1057521725
1000 genomesrs1057521725
hgdprs1057521725
ensemblrs1057521725
gopubmedrs1057521725
geneviewrs1057521725
scholarrs1057521725
googlers1057521725
pharmgkbrs1057521725
gwascentralrs1057521725
openSNPrs1057521725
23andMers1057521725
23andMe allrs1057521725
SNPshotrs1057521725
SNPdbers1057521725
MSV3drs1057521725
GWAS Ctlgrs1057521725
Max Magnitude0
ClinVar
Risk rs1057521725(A;A)
Alt rs1057521725(A;A)
Reference Rs1057521725(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RBFOX1
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.7629861G>A
CLNSRC
CLNACC RCV000443683.1,