rs104894605

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs104894605(C;C)

Make rs104894605(C;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

44007611

Gene

NAGS, PYY

is a	snp
is	mentioned by
dbSNP	rs104894605
dbSNP (classic)	rs104894605
ClinGen	rs104894605
ebi	rs104894605
HLI	rs104894605
Exac	rs104894605
Gnomad	rs104894605
Varsome	rs104894605
LitVar	rs104894605
Map	rs104894605
PheGenI	rs104894605
Biobank	rs104894605
1000 genomes	rs104894605
hgdp	rs104894605
ensembl	rs104894605
geneview	rs104894605
scholar	rs104894605
google	rs104894605
pharmgkb	rs104894605
gwascentral	rs104894605
openSNP	rs104894605
23andMe	rs104894605
SNPshot	rs104894605
SNPdbe	rs104894605
MSV3d	rs104894605
GWAS Ctlg	rs104894605

Max Magnitude

0

OMIM	608300
Desc
Variant	0006
Related	also

ClinVar
Risk	rs104894605(C;C)
Alt	rs104894605(C;C)
Reference	Rs104894605(T;T)
Significance	Pathogenic
Disease	Hyperammonemia
Variation	info
Gene	NAGS
CLNDBN	Hyperammonemia, type III
Reversed	0
HGVS	NC_000017.10:g.42084979T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002534.3,