Have questions? Visit https://www.reddit.com/r/SNPedia

rs796051935

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051935(A;A)
Make rs796051935(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position130464132
GeneASS1
is asnp
is mentioned by
dbSNPrs796051935
ebirs796051935
HLIrs796051935
Exacrs796051935
Varsomers796051935
Maprs796051935
PheGenIrs796051935
hapmaprs796051935
1000 genomesrs796051935
hgdprs796051935
ensemblrs796051935
gopubmedrs796051935
geneviewrs796051935
scholarrs796051935
googlers796051935
pharmgkbrs796051935
gwascentralrs796051935
openSNPrs796051935
23andMers796051935
23andMe allrs796051935
SNP Nexus

SNPshotrs796051935
SNPdbers796051935
MSV3drs796051935
GWAS Ctlgrs796051935
Max Magnitude0
ClinVar
Risk rs796051935(A;A)
Alt rs796051935(A;A)
Reference rs796051935(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASS1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.133339519G>A
CLNSRC
CLNACC RCV000185793.1,