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rs200688856

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200688856(C;C)
Make rs200688856(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position161629989
GeneFCGR3B
is asnp
is mentioned by
dbSNPrs200688856
ebirs200688856
HLIrs200688856
Exacrs200688856
Varsomers200688856
Maprs200688856
PheGenIrs200688856
hapmaprs200688856
1000 genomesrs200688856
hgdprs200688856
ensemblrs200688856
gopubmedrs200688856
geneviewrs200688856
scholarrs200688856
googlers200688856
pharmgkbrs200688856
gwascentralrs200688856
openSNPrs200688856
23andMers200688856
23andMe allrs200688856
SNP Nexus

SNPshotrs200688856
SNPdbers200688856
MSV3drs200688856
GWAS Ctlgrs200688856
Max Magnitude0
ClinVar
Risk rs200688856(A,C;A,C)
Alt rs200688856(A,C;A,C)
Reference rs200688856(G;G)
Significance Pathogenic
Disease Neutrophil-specific antigens na1/na2
Variation info
Gene FCGR3B
CLNDBN Neutrophil-specific antigens na1/na2
Reversed 0
HGVS NC_000001.10:g.161599779G\x3d
CLNSRC OMIM Allelic Variant
CLNACC RCV000030607.2,