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rs797045306

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045306(A;T)
Make rs797045306(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position97864333
GeneASNS
is asnp
is mentioned by
dbSNPrs797045306
ebirs797045306
HLIrs797045306
Exacrs797045306
Varsomers797045306
Maprs797045306
PheGenIrs797045306
hapmaprs797045306
1000 genomesrs797045306
hgdprs797045306
ensemblrs797045306
gopubmedrs797045306
geneviewrs797045306
scholarrs797045306
googlers797045306
pharmgkbrs797045306
gwascentralrs797045306
openSNPrs797045306
23andMers797045306
23andMe allrs797045306
SNP Nexus

SNPshotrs797045306
SNPdbers797045306
MSV3drs797045306
GWAS Ctlgrs797045306
Max Magnitude0
ClinVar
Risk rs797045306(T;T)
Alt rs797045306(T;T)
Reference rs797045306(A;A)
Significance Pathogenic
Disease Asparagine synthetase deficiency
Variation info
Gene ASNS
CLNDBN Asparagine synthetase deficiency
Reversed 1
HGVS NC_000007.13:g.97493645T>A
CLNSRC
CLNACC RCV000194969.1,