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rs199999619

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199999619(A;C)
Make rs199999619(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position12899466
GeneGCDH, SYCE2
is asnp
is mentioned by
dbSNPrs199999619
ebirs199999619
HLIrs199999619
Exacrs199999619
Varsomers199999619
Maprs199999619
PheGenIrs199999619
hapmaprs199999619
1000 genomesrs199999619
hgdprs199999619
ensemblrs199999619
gopubmedrs199999619
geneviewrs199999619
scholarrs199999619
googlers199999619
pharmgkbrs199999619
gwascentralrs199999619
openSNPrs199999619
23andMers199999619
23andMe allrs199999619
SNP Nexus

SNPshotrs199999619
SNPdbers199999619
MSV3drs199999619
GWAS Ctlgrs199999619
Max Magnitude0
ClinVar
Risk rs199999619(C;C)
Alt rs199999619(C;C)
Reference rs199999619(A;A)
Significance Pathogenic
Disease Glutaric aciduria
Variation info
Gene SYCE2 GCDH
CLNDBN Glutaric aciduria, type 1
Reversed 0
HGVS NC_000019.9:g.13010280A>C
CLNSRC
CLNACC RCV000174223.1,