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rs1057524584

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524584(A;A)
Make rs1057524584(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position244863955
GeneHNRNPU
is asnp
is mentioned by
dbSNPrs1057524584
dbSNP (old)rs1057524584
ClinGenrs1057524584
ebirs1057524584
HLIrs1057524584
Exacrs1057524584
Gnomadrs1057524584
Varsomers1057524584
Maprs1057524584
PheGenIrs1057524584
Biobankrs1057524584
1000 genomesrs1057524584
hgdprs1057524584
ensemblrs1057524584
gopubmedrs1057524584
geneviewrs1057524584
scholarrs1057524584
googlers1057524584
pharmgkbrs1057524584
gwascentralrs1057524584
openSNPrs1057524584
23andMers1057524584
23andMe allrs1057524584
SNPshotrs1057524584
SNPdbers1057524584
MSV3drs1057524584
GWAS Ctlgrs1057524584
Max Magnitude0
ClinVar
Risk rs1057524584(A;A)
Alt rs1057524584(A;A)
Reference Rs1057524584(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene HNRNPU
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.245027257G>T
CLNSRC
CLNACC RCV000424048.1,