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rs1057520065

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057520065(-;G)
Make rs1057520065(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position244863679
GeneHNRNPU
is asnp
is mentioned by
dbSNPrs1057520065
dbSNP (classic)rs1057520065
ClinGenrs1057520065
ebirs1057520065
HLIrs1057520065
Exacrs1057520065
Gnomadrs1057520065
Varsomers1057520065
LitVarrs1057520065
Maprs1057520065
PheGenIrs1057520065
Biobankrs1057520065
1000 genomesrs1057520065
hgdprs1057520065
ensemblrs1057520065
geneviewrs1057520065
scholarrs1057520065
googlers1057520065
pharmgkbrs1057520065
gwascentralrs1057520065
openSNPrs1057520065
23andMers1057520065
23andMe allrs1057520065
SNPshotrs1057520065
SNPdbers1057520065
MSV3drs1057520065
GWAS Ctlgrs1057520065
Max Magnitude0
ClinVar
Risk rs1057520065(G;G)
Alt rs1057520065(G;G)
Reference Rs1057520065(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene HNRNPU
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.245026982dupC
CLNSRC
CLNACC RCV000433810.1,