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rs121907951

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121907951(C;G)
Make rs121907951(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position57602081
GeneSERPING1
is asnp
is mentioned by
dbSNPrs121907951
ebirs121907951
HLIrs121907951
Exacrs121907951
Varsomers121907951
Maprs121907951
PheGenIrs121907951
hapmaprs121907951
1000 genomesrs121907951
hgdprs121907951
ensemblrs121907951
gopubmedrs121907951
geneviewrs121907951
scholarrs121907951
googlers121907951
pharmgkbrs121907951
gwascentralrs121907951
openSNPrs121907951
23andMers121907951
23andMe allrs121907951
SNP Nexus

SNPshotrs121907951
SNPdbers121907951
MSV3drs121907951
GWAS Ctlgrs121907951
Max Magnitude0
OMIM606860
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121907951(G;G)
Alt rs121907951(G;G)
Reference rs121907951(C;C)
Significance Pathogenic
Disease Hereditary angioedema type 1
Variation info
Gene SERPING1
CLNDBN Hereditary angioedema type 1
Reversed 0
HGVS NC_000011.9:g.57369554C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000004163.2,