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rs138946894

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs138946894(A;A)
Make rs138946894(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position247423853
GeneNLRP3
is asnp
is mentioned by
dbSNPrs138946894
ebirs138946894
HLIrs138946894
Exacrs138946894
Varsomers138946894
Maprs138946894
PheGenIrs138946894
hapmaprs138946894
1000 genomesrs138946894
hgdprs138946894
ensemblrs138946894
gopubmedrs138946894
geneviewrs138946894
scholarrs138946894
googlers138946894
pharmgkbrs138946894
gwascentralrs138946894
openSNPrs138946894
23andMers138946894
23andMe allrs138946894
SNP Nexus

SNPshotrs138946894
SNPdbers138946894
MSV3drs138946894
GWAS Ctlgrs138946894
Max Magnitude0
ClinVar
Risk rs138946894(A,C;A,C)
Alt rs138946894(A,C;A,C)
Reference rs138946894(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NLRP3
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.247587155G>A
CLNSRC
CLNACC RCV000219739.1,