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rs35937854

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs35937854(C;C)
Make rs35937854(C;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position183566954
GeneNCF2
is asnp
is mentioned by
dbSNPrs35937854
dbSNP (old)rs35937854
ClinGenrs35937854
ebirs35937854
HLIrs35937854
Exacrs35937854
Gnomadrs35937854
Varsomers35937854
Maprs35937854
PheGenIrs35937854
Biobankrs35937854
1000 genomesrs35937854
hgdprs35937854
ensemblrs35937854
gopubmedrs35937854
geneviewrs35937854
scholarrs35937854
googlers35937854
pharmgkbrs35937854
gwascentralrs35937854
openSNPrs35937854
23andMers35937854
23andMe allrs35937854
SNP Nexus

SNPshotrs35937854
SNPdbers35937854
MSV3drs35937854
GWAS Ctlgrs35937854
GMAF0.009642
Max Magnitude0

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

ClinVar
Risk rs35937854(C;C)
Alt rs35937854(C;C)
Reference Rs35937854(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene NCF2
CLNDBN not specified
Reversed 1
HGVS NC_000001.10:g.183536089A>G
CLNSRC
CLNACC RCV000317093.1,