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rs765338121

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs765338121(A;A)
Make rs765338121(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130489341
GeneASS1
is asnp
is mentioned by
dbSNPrs765338121
dbSNP (classic)rs765338121
ClinGenrs765338121
ebirs765338121
HLIrs765338121
Exacrs765338121
Gnomadrs765338121
Varsomers765338121
LitVarrs765338121
Maprs765338121
PheGenIrs765338121
Biobankrs765338121
1000 genomesrs765338121
hgdprs765338121
ensemblrs765338121
geneviewrs765338121
scholarrs765338121
googlers765338121
pharmgkbrs765338121
gwascentralrs765338121
openSNPrs765338121
23andMers765338121
23andMe allrs765338121
SNPshotrs765338121
SNPdbers765338121
MSV3drs765338121
GWAS Ctlgrs765338121
Max Magnitude0
ClinVar
Risk rs765338121(A;A)
Alt rs765338121(A;A)
Reference Rs765338121(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASS1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.133364728G>A
CLNSRC
CLNACC RCV000493705.1,