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rs730880303

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730880303(-;-)
Make rs730880303(-;T)
Make rs730880303(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position44007629
GeneNAGS, PYY
is asnp
is mentioned by
dbSNPrs730880303
ebirs730880303
HLIrs730880303
Exacrs730880303
Varsomers730880303
Maprs730880303
PheGenIrs730880303
hapmaprs730880303
1000 genomesrs730880303
hgdprs730880303
ensemblrs730880303
gopubmedrs730880303
geneviewrs730880303
scholarrs730880303
googlers730880303
pharmgkbrs730880303
gwascentralrs730880303
openSNPrs730880303
23andMers730880303
23andMe allrs730880303
SNP Nexus

SNPshotrs730880303
SNPdbers730880303
MSV3drs730880303
GWAS Ctlgrs730880303
Max Magnitude0
ClinVar
Risk rs730880303(T;T)
Alt rs730880303(T;T)
Reference rs730880303(;)
Significance Pathogenic
Disease Hyperammonemia
Variation info
Gene NAGS
CLNDBN Hyperammonemia, type III
Reversed 0
HGVS NC_000017.10:g.42084997dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000002532.3,