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rs1057520752

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520752(A;A)
Make rs1057520752(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position54124657
GenePRPF31
is asnp
is mentioned by
dbSNPrs1057520752
dbSNP (old)rs1057520752
ClinGenrs1057520752
ebirs1057520752
HLIrs1057520752
Exacrs1057520752
Gnomadrs1057520752
Varsomers1057520752
Maprs1057520752
PheGenIrs1057520752
Biobankrs1057520752
1000 genomesrs1057520752
hgdprs1057520752
ensemblrs1057520752
gopubmedrs1057520752
geneviewrs1057520752
scholarrs1057520752
googlers1057520752
pharmgkbrs1057520752
gwascentralrs1057520752
openSNPrs1057520752
23andMers1057520752
23andMe allrs1057520752
SNPshotrs1057520752
SNPdbers1057520752
MSV3drs1057520752
GWAS Ctlgrs1057520752
Max Magnitude0
ClinVar
Risk rs1057520752(A;A)
Alt rs1057520752(A;A)
Reference Rs1057520752(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PRPF31
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.54628036G>A
CLNSRC
CLNACC RCV000437897.1,