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rs749908889

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs749908889(C;T)
Make rs749908889(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position136329946
GenePCCB
is asnp
is mentioned by
dbSNPrs749908889
ebirs749908889
HLIrs749908889
Exacrs749908889
Varsomers749908889
Maprs749908889
PheGenIrs749908889
hapmaprs749908889
1000 genomesrs749908889
hgdprs749908889
ensemblrs749908889
gopubmedrs749908889
geneviewrs749908889
scholarrs749908889
googlers749908889
pharmgkbrs749908889
gwascentralrs749908889
openSNPrs749908889
23andMers749908889
23andMe allrs749908889
SNP Nexus

SNPshotrs749908889
SNPdbers749908889
MSV3drs749908889
GWAS Ctlgrs749908889
Max Magnitude0
ClinVar
Risk rs749908889(T;T)
Alt rs749908889(T;T)
Reference rs749908889(C;C)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.136048788C>T
CLNSRC
CLNACC RCV000235647.1,