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rs760387660

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs760387660(A;A)
Make rs760387660(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position100157339
GenePCCA
is asnp
is mentioned by
dbSNPrs760387660
ebirs760387660
HLIrs760387660
Exacrs760387660
Varsomers760387660
Maprs760387660
PheGenIrs760387660
hapmaprs760387660
1000 genomesrs760387660
hgdprs760387660
ensemblrs760387660
gopubmedrs760387660
geneviewrs760387660
scholarrs760387660
googlers760387660
pharmgkbrs760387660
gwascentralrs760387660
openSNPrs760387660
23andMers760387660
23andMe allrs760387660
SNP Nexus

SNPshotrs760387660
SNPdbers760387660
MSV3drs760387660
GWAS Ctlgrs760387660
Max Magnitude0
ClinVar
Risk rs760387660(A;A)
Alt rs760387660(A;A)
Reference rs760387660(T;T)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCA
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000013.10:g.100809593T>A
CLNSRC
CLNACC RCV000235728.1,