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rs768703749

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768703749(A;A)
Make rs768703749(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position100309905
GenePCCA
is asnp
is mentioned by
dbSNPrs768703749
ebirs768703749
HLIrs768703749
Exacrs768703749
Varsomers768703749
Maprs768703749
PheGenIrs768703749
hapmaprs768703749
1000 genomesrs768703749
hgdprs768703749
ensemblrs768703749
gopubmedrs768703749
geneviewrs768703749
scholarrs768703749
googlers768703749
pharmgkbrs768703749
gwascentralrs768703749
openSNPrs768703749
23andMers768703749
23andMe allrs768703749
SNP Nexus

SNPshotrs768703749
SNPdbers768703749
MSV3drs768703749
GWAS Ctlgrs768703749
Max Magnitude0
ClinVar
Risk rs768703749(A,T;A,T)
Alt rs768703749(A,T;A,T)
Reference rs768703749(C;C)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCA
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000013.10:g.100962159C>T
CLNSRC
CLNACC RCV000236395.1,