rs151344629

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs151344629(C;T)

Make rs151344629(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

247424492

Gene

NLRP3

is a	snp
is	mentioned by
dbSNP	rs151344629
dbSNP (classic)	rs151344629
ClinGen	rs151344629
ebi	rs151344629
HLI	rs151344629
Exac	rs151344629
Gnomad	rs151344629
Varsome	rs151344629
LitVar	rs151344629
Map	rs151344629
PheGenI	rs151344629
Biobank	rs151344629
1000 genomes	rs151344629
hgdp	rs151344629
ensembl	rs151344629
geneview	rs151344629
scholar	rs151344629
google	rs151344629
pharmgkb	rs151344629
gwascentral	rs151344629
openSNP	rs151344629
23andMe	rs151344629
SNPshot	rs151344629
SNPdbe	rs151344629
MSV3d	rs151344629
GWAS Ctlg	rs151344629

Max Magnitude

0

ClinVar
Risk	rs151344629(T;T)
Alt	rs151344629(T;T)
Reference	Rs151344629(C;C)
Significance	Pathogenic
Disease	Familial cold urticaria not provided Familial amyloid nephropathy with urticaria AND deafness
Variation	info
Gene	NLRP3
CLNDBN	Familial cold urticaria not provided Familial amyloid nephropathy with urticaria AND deafness
Reversed	0
HGVS	NC_000001.10:g.247587794C>T
CLNSRC
CLNACC	RCV000084167.1, RCV000214584.2, RCV000449533.1,