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rs869312701

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312701(C;T)
Make rs869312701(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position244864241
GeneHNRNPU
is asnp
is mentioned by
dbSNPrs869312701
ebirs869312701
HLIrs869312701
Exacrs869312701
Varsomers869312701
Maprs869312701
PheGenIrs869312701
hapmaprs869312701
1000 genomesrs869312701
hgdprs869312701
ensemblrs869312701
gopubmedrs869312701
geneviewrs869312701
scholarrs869312701
googlers869312701
pharmgkbrs869312701
gwascentralrs869312701
openSNPrs869312701
23andMers869312701
23andMe allrs869312701
SNP Nexus

SNPshotrs869312701
SNPdbers869312701
MSV3drs869312701
GWAS Ctlgrs869312701
Max Magnitude0
ClinVar
Risk rs869312701(T;T)
Alt rs869312701(T;T)
Reference rs869312701(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HNRNPU
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.245027543G>A
CLNSRC
CLNACC RCV000209838.1,