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rs121909617

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909617(A;A)
Make rs121909617(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154569648
GeneFGB
is asnp
is mentioned by
dbSNPrs121909617
ebirs121909617
HLIrs121909617
Exacrs121909617
Varsomers121909617
Maprs121909617
PheGenIrs121909617
hapmaprs121909617
1000 genomesrs121909617
hgdprs121909617
ensemblrs121909617
gopubmedrs121909617
geneviewrs121909617
scholarrs121909617
googlers121909617
pharmgkbrs121909617
gwascentralrs121909617
openSNPrs121909617
23andMers121909617
23andMe allrs121909617
SNP Nexus

SNPshotrs121909617
SNPdbers121909617
MSV3drs121909617
GWAS Ctlgrs121909617
Max Magnitude0
OMIM134830
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909617(A;A)
Alt rs121909617(A;A)
Reference rs121909617(G;G)
Significance Other
Disease FIBRINOGEN PONTOISE 2
Variation info
Gene FGB
CLNDBN FIBRINOGEN PONTOISE 2
Reversed 0
HGVS NC_000004.11:g.155490800G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017807.1,