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rs1057524777

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524777(C;C)
Make rs1057524777(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position247424368
GeneNLRP3
is asnp
is mentioned by
dbSNPrs1057524777
dbSNP (classic)rs1057524777
ClinGenrs1057524777
ebirs1057524777
HLIrs1057524777
Exacrs1057524777
Gnomadrs1057524777
Varsomers1057524777
LitVarrs1057524777
Maprs1057524777
PheGenIrs1057524777
Biobankrs1057524777
1000 genomesrs1057524777
hgdprs1057524777
ensemblrs1057524777
geneviewrs1057524777
scholarrs1057524777
googlers1057524777
pharmgkbrs1057524777
gwascentralrs1057524777
openSNPrs1057524777
23andMers1057524777
23andMe allrs1057524777
SNPshotrs1057524777
SNPdbers1057524777
MSV3drs1057524777
GWAS Ctlgrs1057524777
Max Magnitude0
ClinVar
Risk rs1057524777(C;C)
Alt rs1057524777(C;C)
Reference Rs1057524777(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NLRP3
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.247587670G>C
CLNSRC
CLNACC RCV000437559.1,