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rs1057524408

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524408(C;T)
Make rs1057524408(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position71290740
GeneNONO
is asnp
is mentioned by
dbSNPrs1057524408
dbSNP (old)rs1057524408
ClinGenrs1057524408
ebirs1057524408
HLIrs1057524408
Exacrs1057524408
Gnomadrs1057524408
Varsomers1057524408
LitVarrs1057524408
Maprs1057524408
PheGenIrs1057524408
Biobankrs1057524408
1000 genomesrs1057524408
hgdprs1057524408
ensemblrs1057524408
gopubmedrs1057524408
geneviewrs1057524408
scholarrs1057524408
googlers1057524408
pharmgkbrs1057524408
gwascentralrs1057524408
openSNPrs1057524408
23andMers1057524408
23andMe allrs1057524408
SNPshotrs1057524408
SNPdbers1057524408
MSV3drs1057524408
GWAS Ctlgrs1057524408
Max Magnitude0
ClinVar
Risk rs1057524408(T;T)
Alt rs1057524408(T;T)
Reference Rs1057524408(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NONO
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70510590C>T
CLNSRC
CLNACC RCV000435263.1,