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rs28445840

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28445840(A;A)
Make rs28445840(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position36864918
GeneLOC107985578, NCF4
is asnp
is mentioned by
dbSNPrs28445840
dbSNP (classic)rs28445840
ClinGenrs28445840
ebirs28445840
HLIrs28445840
Exacrs28445840
Gnomadrs28445840
Varsomers28445840
LitVarrs28445840
Maprs28445840
PheGenIrs28445840
Biobankrs28445840
1000 genomesrs28445840
hgdprs28445840
ensemblrs28445840
geneviewrs28445840
scholarrs28445840
googlers28445840
pharmgkbrs28445840
gwascentralrs28445840
openSNPrs28445840
23andMers28445840
23andMe allrs28445840
SNPshotrs28445840
SNPdbers28445840
MSV3drs28445840
GWAS Ctlgrs28445840
Max Magnitude0
ClinVar
Risk rs28445840(A;A)
Alt rs28445840(A;A)
Reference Rs28445840(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NCF4
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.37260960G>A
CLNSRC
CLNACC RCV000488142.1,