Have questions? Visit https://www.reddit.com/r/SNPedia

rs138149179

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs138149179(C;T)
Make rs138149179(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position100273218
GenePCCA
is asnp
is mentioned by
dbSNPrs138149179
ebirs138149179
HLIrs138149179
Exacrs138149179
Varsomers138149179
Maprs138149179
PheGenIrs138149179
hapmaprs138149179
1000 genomesrs138149179
hgdprs138149179
ensemblrs138149179
gopubmedrs138149179
geneviewrs138149179
scholarrs138149179
googlers138149179
pharmgkbrs138149179
gwascentralrs138149179
openSNPrs138149179
23andMers138149179
23andMe allrs138149179
SNP Nexus

SNPshotrs138149179
SNPdbers138149179
MSV3drs138149179
GWAS Ctlgrs138149179
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs138149179(T;T)
Alt rs138149179(T;T)
Reference rs138149179(C;C)
Significance Pathogenic
Disease Propionic acidemia not provided
Variation info
Gene PCCA
CLNDBN Propionic acidemia not provided
Reversed 0
HGVS NC_000013.10:g.100925472C>T
CLNSRC HGMD
CLNACC RCV000032113.3, RCV000078552.3,