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rs183276875

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs183276875(C;T)
Make rs183276875(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position130489413
GeneASS1
is asnp
is mentioned by
dbSNPrs183276875
dbSNP (old)rs183276875
ClinGenrs183276875
ebirs183276875
HLIrs183276875
Exacrs183276875
Gnomadrs183276875
Varsomers183276875
LitVarrs183276875
Maprs183276875
PheGenIrs183276875
Biobankrs183276875
1000 genomesrs183276875
hgdprs183276875
ensemblrs183276875
gopubmedrs183276875
geneviewrs183276875
scholarrs183276875
googlers183276875
pharmgkbrs183276875
gwascentralrs183276875
openSNPrs183276875
23andMers183276875
23andMe allrs183276875
SNPshotrs183276875
SNPdbers183276875
MSV3drs183276875
GWAS Ctlgrs183276875
Max Magnitude0
ClinVar
Risk rs183276875(T;T)
Alt rs183276875(T;T)
Reference Rs183276875(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASS1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.133364800C>T
CLNSRC
CLNACC RCV000255358.1,