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rs730880267

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880267(A;T)
Make rs730880267(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position44006527
GeneNAGS, PYY
is asnp
is mentioned by
dbSNPrs730880267
ebirs730880267
HLIrs730880267
Exacrs730880267
Varsomers730880267
Maprs730880267
PheGenIrs730880267
hapmaprs730880267
1000 genomesrs730880267
hgdprs730880267
ensemblrs730880267
gopubmedrs730880267
geneviewrs730880267
scholarrs730880267
googlers730880267
pharmgkbrs730880267
gwascentralrs730880267
openSNPrs730880267
23andMers730880267
23andMe allrs730880267
SNP Nexus

SNPshotrs730880267
SNPdbers730880267
MSV3drs730880267
GWAS Ctlgrs730880267
Max Magnitude0
ClinVar
Risk rs730880267(T;T)
Alt rs730880267(T;T)
Reference rs730880267(A;A)
Significance Pathogenic
Disease Hyperammonemia
Variation info
Gene NAGS
CLNDBN Hyperammonemia, type III
Reversed 0
HGVS NC_000017.10:g.42083895A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002531.3,