Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909618

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909618(G;T)
Make rs121909618(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154565826
GeneFGB
is asnp
is mentioned by
dbSNPrs121909618
ebirs121909618
HLIrs121909618
Exacrs121909618
Varsomers121909618
Maprs121909618
PheGenIrs121909618
hapmaprs121909618
1000 genomesrs121909618
hgdprs121909618
ensemblrs121909618
gopubmedrs121909618
geneviewrs121909618
scholarrs121909618
googlers121909618
pharmgkbrs121909618
gwascentralrs121909618
openSNPrs121909618
23andMers121909618
23andMe allrs121909618
SNP Nexus

SNPshotrs121909618
SNPdbers121909618
MSV3drs121909618
GWAS Ctlgrs121909618
Max Magnitude0
OMIM134830
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909618(T;T)
Alt rs121909618(T;T)
Reference rs121909618(G;G)
Significance Other
Disease FIBRINOGEN ISE
Variation info
Gene FGB
CLNDBN FIBRINOGEN ISE
Reversed 0
HGVS NC_000004.11:g.155486978G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017809.2,