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rs796051934

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796051934(A;A)
Make rs796051934(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position130452328
GeneASS1
is asnp
is mentioned by
dbSNPrs796051934
ebirs796051934
HLIrs796051934
Exacrs796051934
Varsomers796051934
Maprs796051934
PheGenIrs796051934
hapmaprs796051934
1000 genomesrs796051934
hgdprs796051934
ensemblrs796051934
gopubmedrs796051934
geneviewrs796051934
scholarrs796051934
googlers796051934
pharmgkbrs796051934
gwascentralrs796051934
openSNPrs796051934
23andMers796051934
23andMe allrs796051934
SNP Nexus

SNPshotrs796051934
SNPdbers796051934
MSV3drs796051934
GWAS Ctlgrs796051934
Max Magnitude0
ClinVar
Risk rs796051934(A;A)
Alt rs796051934(A;A)
Reference rs796051934(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASS1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.133327715T>A
CLNSRC
CLNACC RCV000185792.1,