Have questions? Visit https://www.reddit.com/r/SNPedia

rs6672995

From SNPedia

Orientationplus
Stabilizedplus
Make rs6672995(A;A)
Make rs6672995(A;G)
Make rs6672995(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position247457731
is asnp
is mentioned by
dbSNPrs6672995
ebirs6672995
HLIrs6672995
Exacrs6672995
Varsomers6672995
Maprs6672995
PheGenIrs6672995
hapmaprs6672995
1000 genomesrs6672995
hgdprs6672995
ensemblrs6672995
gopubmedrs6672995
geneviewrs6672995
scholarrs6672995
googlers6672995
pharmgkbrs6672995
gwascentralrs6672995
openSNPrs6672995
23andMers6672995
23andMe allrs6672995
SNP Nexus

SNPshotrs6672995
SNPdbers6672995
MSV3drs6672995
GWAS Ctlgrs6672995
GMAF0.1322
Max Magnitude
? (A;A) (A;G) (G;G) 28
OMIM606416
DescNLR FAMILY, PYRIN DOMAIN-CONTAINING 3; NLRP3
Variant
Relatedalso
OMIM266600
Desc
Variant
Relatedalso
[PMID 19098911OA-icon.png] 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.