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rs796051936

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796051936(C;C)
Make rs796051936(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position130471502
GeneASS1
is asnp
is mentioned by
dbSNPrs796051936
ebirs796051936
HLIrs796051936
Exacrs796051936
Varsomers796051936
Maprs796051936
PheGenIrs796051936
hapmaprs796051936
1000 genomesrs796051936
hgdprs796051936
ensemblrs796051936
gopubmedrs796051936
geneviewrs796051936
scholarrs796051936
googlers796051936
pharmgkbrs796051936
gwascentralrs796051936
openSNPrs796051936
23andMers796051936
23andMe allrs796051936
SNP Nexus

SNPshotrs796051936
SNPdbers796051936
MSV3drs796051936
GWAS Ctlgrs796051936
Max Magnitude0
ClinVar
Risk rs796051936(C;C)
Alt rs796051936(C;C)
Reference rs796051936(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASS1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.133346889T>C
CLNSRC
CLNACC RCV000185794.1,