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rs121909620

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909620(A;A)
Make rs121909620(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154565985
GeneFGB
is asnp
is mentioned by
dbSNPrs121909620
ebirs121909620
HLIrs121909620
Exacrs121909620
Varsomers121909620
Maprs121909620
PheGenIrs121909620
hapmaprs121909620
1000 genomesrs121909620
hgdprs121909620
ensemblrs121909620
gopubmedrs121909620
geneviewrs121909620
scholarrs121909620
googlers121909620
pharmgkbrs121909620
gwascentralrs121909620
openSNPrs121909620
23andMers121909620
23andMe allrs121909620
SNP Nexus

SNPshotrs121909620
SNPdbers121909620
MSV3drs121909620
GWAS Ctlgrs121909620
Max Magnitude0
OMIM134830
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121909620(A;A)
Alt rs121909620(A;A)
Reference rs121909620(G;G)
Significance Other
Disease FIBRINOGEN NAPLES
Variation info
Gene FGB
CLNDBN FIBRINOGEN NAPLES
Reversed 0
HGVS NC_000004.11:g.155487137G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017811.5,