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rs796051935

From SNPedia

Orientationplus
Stabilizedplus
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
dbSNP (classic)rs796051935
ClinGenrs796051935
ebirs796051935
HLIrs796051935
Exacrs796051935
Gnomadrs796051935
Varsomers796051935
LitVarrs796051935
Maprs796051935
PheGenIrs796051935
Biobankrs796051935
1000 genomesrs796051935
hgdprs796051935
ensemblrs796051935
geneviewrs796051935
scholarrs796051935
googlers796051935
pharmgkbrs796051935
gwascentralrs796051935
openSNPrs796051935
23andMers796051935
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,