rs6672995

Orientation

plus

Stabilized

plus

Make rs6672995(A;A)

Make rs6672995(A;G)

Make rs6672995(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

247457731

is a	snp
is	mentioned by
dbSNP	rs6672995
dbSNP (classic)	rs6672995
ClinGen	rs6672995
ebi	rs6672995
HLI	rs6672995
Exac	rs6672995
Gnomad	rs6672995
Varsome	rs6672995
LitVar	rs6672995
Map	rs6672995
PheGenI	rs6672995
Biobank	rs6672995
1000 genomes	rs6672995
hgdp	rs6672995
ensembl	rs6672995
geneview	rs6672995
scholar	rs6672995
google	rs6672995
pharmgkb	rs6672995
gwascentral	rs6672995
openSNP	rs6672995
23andMe	rs6672995
SNPshot	rs6672995
SNPdbe	rs6672995
MSV3d	rs6672995
GWAS Ctlg	rs6672995

GMAF

0.1322

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

OMIM	606416
Desc	NLR FAMILY, PYRIN DOMAIN-CONTAINING 3; NLRP3
Variant
Related	also

OMIM	266600
Desc
Variant
Related	also

[PMID 19098911] Common variants in the NLRP3 region contribute to Crohn's disease susceptibility.

[PMID 27819323] Donor and recipient genetic variants in NLRP3 associate with early acute rejection following kidney transplantation.