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rs28941477

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs28941477(A;A)
Make rs28941477(A;G)
ReferenceGRCh37 37.1/131
Chromosome7
Position72637963
GeneNCF1B
is asnp
is mentioned by
dbSNPrs28941477
ebirs28941477
HLIrs28941477
Exacrs28941477
Varsomers28941477
Maprs28941477
PheGenIrs28941477
hapmaprs28941477
1000 genomesrs28941477
hgdprs28941477
ensemblrs28941477
gopubmedrs28941477
geneviewrs28941477
scholarrs28941477
googlers28941477
pharmgkbrs28941477
gwascentralrs28941477
openSNPrs28941477
23andMers28941477
23andMe allrs28941477
SNP Nexus

SNPshotrs28941477
SNPdbers28941477
MSV3drs28941477
GWAS Ctlgrs28941477
StatusDeleted
Max Magnitude0
OMIM608512
DescGRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I
Variant0003
Relatedalso