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rs770362721

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs770362721(-;-)
Make rs770362721(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position130489386
GeneASS1
is asnp
is mentioned by
dbSNPrs770362721
ebirs770362721
HLIrs770362721
Exacrs770362721
Varsomers770362721
Maprs770362721
PheGenIrs770362721
hapmaprs770362721
1000 genomesrs770362721
hgdprs770362721
ensemblrs770362721
gopubmedrs770362721
geneviewrs770362721
scholarrs770362721
googlers770362721
pharmgkbrs770362721
gwascentralrs770362721
openSNPrs770362721
23andMers770362721
23andMe allrs770362721
SNP Nexus

SNPshotrs770362721
SNPdbers770362721
MSV3drs770362721
GWAS Ctlgrs770362721
Max Magnitude0
ClinVar
Risk rs770362721(;)
Alt rs770362721(;)
Reference rs770362721(G;G)
Significance Probable-Pathogenic
Disease Citrullinemia type I
Variation info
Gene ASS1
CLNDBN Citrullinemia type I
Reversed 0
HGVS NC_000009.11:g.133364773delG
CLNSRC
CLNACC RCV000169181.1,