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rs373824502

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373824502(C;T)
Make rs373824502(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position244841992
GeneCOX20, HNRNPU-AS1
is asnp
is mentioned by
dbSNPrs373824502
ebirs373824502
HLIrs373824502
Exacrs373824502
Varsomers373824502
Maprs373824502
PheGenIrs373824502
hapmaprs373824502
1000 genomesrs373824502
hgdprs373824502
ensemblrs373824502
gopubmedrs373824502
geneviewrs373824502
scholarrs373824502
googlers373824502
pharmgkbrs373824502
gwascentralrs373824502
openSNPrs373824502
23andMers373824502
23andMe allrs373824502
SNP Nexus

SNPshotrs373824502
SNPdbers373824502
MSV3drs373824502
GWAS Ctlgrs373824502
Max Magnitude0
ClinVar
Risk rs373824502(A,T;A,T)
Alt rs373824502(A,T;A,T)
Reference rs373824502(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HNRNPU-AS1 COX20
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.245005294C>T
CLNSRC
CLNACC RCV000198658.1,