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rs606231460

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs606231460(A;C)
Make rs606231460(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position32250536
GeneNLRC4
is asnp
is mentioned by
dbSNPrs606231460
ebirs606231460
HLIrs606231460
Exacrs606231460
Varsomers606231460
Maprs606231460
PheGenIrs606231460
hapmaprs606231460
1000 genomesrs606231460
hgdprs606231460
ensemblrs606231460
gopubmedrs606231460
geneviewrs606231460
scholarrs606231460
googlers606231460
pharmgkbrs606231460
gwascentralrs606231460
openSNPrs606231460
23andMers606231460
23andMe allrs606231460
SNP Nexus

SNPshotrs606231460
SNPdbers606231460
MSV3drs606231460
GWAS Ctlgrs606231460
Max Magnitude0
ClinVar
Risk rs606231460(C;C)
Alt rs606231460(C;C)
Reference rs606231460(A;A)
Significance Pathogenic
Disease Familial cold autoinflammatory syndrome 4
Variation info
Gene NLRC4
CLNDBN Familial cold autoinflammatory syndrome 4
Reversed 1
HGVS NC_000002.11:g.32475605T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000148929.5,