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rs58599399

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs58599399(G;T)
Make rs58599399(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position49295621
GenePRPH, RP11-161H23.9
is asnp
is mentioned by
dbSNPrs58599399
ebirs58599399
HLIrs58599399
Exacrs58599399
Varsomers58599399
Maprs58599399
PheGenIrs58599399
hapmaprs58599399
1000 genomesrs58599399
hgdprs58599399
ensemblrs58599399
gopubmedrs58599399
geneviewrs58599399
scholarrs58599399
googlers58599399
pharmgkbrs58599399
gwascentralrs58599399
openSNPrs58599399
23andMers58599399
23andMe allrs58599399
SNP Nexus

SNPshotrs58599399
SNPdbers58599399
MSV3drs58599399
GWAS Ctlgrs58599399
GMAF0.001377
Max Magnitude0
OMIM170710
Desc
Variant0002
Relatedalso


ClinVar
Risk rs58599399(T;T)
Alt rs58599399(T;T)
Reference rs58599399(G;G)
Significance Other
Disease Amyotrophic lateral sclerosis not provided
Variation info
Gene PRPH LOC101927267 RP11-161H23.9
CLNDBN Amyotrophic lateral sclerosis, susceptibility to not provided
Reversed 0
HGVS NC_000012.11:g.49689404G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014706.2, RCV000057167.1,