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rs373359894

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs373359894(A;A)
Make rs373359894(A;G)
ReferenceGRCh38 38.1/142
Chromosome9
Position120997684
GeneC5
is asnp
is mentioned by
dbSNPrs373359894
ebirs373359894
HLIrs373359894
Exacrs373359894
Varsomers373359894
Maprs373359894
PheGenIrs373359894
hapmaprs373359894
1000 genomesrs373359894
hgdprs373359894
ensemblrs373359894
gopubmedrs373359894
geneviewrs373359894
scholarrs373359894
googlers373359894
pharmgkbrs373359894
gwascentralrs373359894
openSNPrs373359894
23andMers373359894
23andMe allrs373359894
SNP Nexus

SNPshotrs373359894
SNPdbers373359894
MSV3drs373359894
GWAS Ctlgrs373359894
Max Magnitude0
ClinVar
Risk rs373359894(A,T;A,T)
Alt rs373359894(A,T;A,T)
Reference rs373359894(G;G)
Significance Other
Disease Eculizumab
Variation info
Gene C5
CLNDBN Eculizumab, poor response to
Reversed 0
HGVS NC_000009.11:g.123759962G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000114935.3,