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rs180177465

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs180177465(A;C)
Make rs180177465(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position247424755
GeneNLRP3
is asnp
is mentioned by
dbSNPrs180177465
dbSNP (old)rs180177465
ClinGenrs180177465
ebirs180177465
HLIrs180177465
Exacrs180177465
Gnomadrs180177465
Varsomers180177465
LitVarrs180177465
Maprs180177465
PheGenIrs180177465
Biobankrs180177465
1000 genomesrs180177465
hgdprs180177465
ensemblrs180177465
gopubmedrs180177465
geneviewrs180177465
scholarrs180177465
googlers180177465
pharmgkbrs180177465
gwascentralrs180177465
openSNPrs180177465
23andMers180177465
23andMe allrs180177465
SNPshotrs180177465
SNPdbers180177465
MSV3drs180177465
GWAS Ctlgrs180177465
Max Magnitude0
ClinVar
Risk rs180177465(C;C) rs180177465(G;G)
Alt rs180177465(C;C) rs180177465(G;G)
Reference Rs180177465(A;A)
Significance Probable-Pathogenic
Disease Familial cold urticaria not provided
Variation info
Gene NLRP3
CLNDBN Familial cold urticaria not provided
Reversed 0
HGVS NC_000001.10:g.247588057A>C; NC_000001.10:g.247588057A>G
CLNSRC
CLNACC RCV000084179.1, RCV000084180.1, RCV000433450.1,