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

rs1057517936

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517936(G;G)
Make rs1057517936(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position13025481
GeneNFIX
is asnp
is mentioned by
dbSNPrs1057517936
dbSNP (old)rs1057517936
ClinGenrs1057517936
ebirs1057517936
HLIrs1057517936
Exacrs1057517936
Gnomadrs1057517936
Varsomers1057517936
Maprs1057517936
PheGenIrs1057517936
Biobankrs1057517936
1000 genomesrs1057517936
hgdprs1057517936
ensemblrs1057517936
gopubmedrs1057517936
geneviewrs1057517936
scholarrs1057517936
googlers1057517936
pharmgkbrs1057517936
gwascentralrs1057517936
openSNPrs1057517936
23andMers1057517936
23andMe allrs1057517936
SNPshotrs1057517936
SNPdbers1057517936
MSV3drs1057517936
GWAS Ctlgrs1057517936
Max Magnitude0
ClinVar
Risk rs1057517936(G;G)
Alt rs1057517936(G;G)
Reference Rs1057517936(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NFIX
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.13136295T>G
CLNSRC
CLNACC RCV000413589.1,