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rs17849501

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17849501(C;T)
Make rs17849501(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position183573188
GeneNCF2
is asnp
is mentioned by
dbSNPrs17849501
ebirs17849501
HLIrs17849501
Exacrs17849501
Varsomers17849501
Maprs17849501
PheGenIrs17849501
hapmaprs17849501
1000 genomesrs17849501
hgdprs17849501
ensemblrs17849501
gopubmedrs17849501
geneviewrs17849501
scholarrs17849501
googlers17849501
pharmgkbrs17849501
gwascentralrs17849501
openSNPrs17849501
23andMers17849501
23andMe allrs17849501
SNP Nexus

SNPshotrs17849501
SNPdbers17849501
MSV3drs17849501
GWAS Ctlgrs17849501
GMAF0.02571
Max Magnitude0

[PMID 24163247OA-icon.png] Allelic heterogeneity in NCF2 associated with systemic lupus erythematosus (SLE) susceptibility across four ethnic populations


ClinVar
Risk rs17849501(T;T)
Alt rs17849501(T;T)
Reference rs17849501(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene NCF2
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.183542323C>T
CLNSRC
CLNACC RCV000178768.1,