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rs1057524637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524637(A;T)
Make rs1057524637(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position140114866
GenePURA
is asnp
is mentioned by
dbSNPrs1057524637
dbSNP (classic)rs1057524637
ClinGenrs1057524637
ebirs1057524637
HLIrs1057524637
Exacrs1057524637
Gnomadrs1057524637
Varsomers1057524637
LitVarrs1057524637
Maprs1057524637
PheGenIrs1057524637
Biobankrs1057524637
1000 genomesrs1057524637
hgdprs1057524637
ensemblrs1057524637
geneviewrs1057524637
scholarrs1057524637
googlers1057524637
pharmgkbrs1057524637
gwascentralrs1057524637
openSNPrs1057524637
23andMers1057524637
SNPshotrs1057524637
SNPdbers1057524637
MSV3drs1057524637
GWAS Ctlgrs1057524637
Max Magnitude0
ClinVar
Risk rs1057524637(T;T)
Alt rs1057524637(T;T)
Reference Rs1057524637(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PURA
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.139494451A>T
CLNSRC
CLNACC RCV000445344.1,