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

rs121913088

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913088(A;A)
Make rs121913088(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154606932
GeneFGG
is asnp
is mentioned by
dbSNPrs121913088
ebirs121913088
HLIrs121913088
Exacrs121913088
Varsomers121913088
Maprs121913088
PheGenIrs121913088
hapmaprs121913088
1000 genomesrs121913088
hgdprs121913088
ensemblrs121913088
gopubmedrs121913088
geneviewrs121913088
scholarrs121913088
googlers121913088
pharmgkbrs121913088
gwascentralrs121913088
openSNPrs121913088
23andMers121913088
23andMe allrs121913088
SNP Nexus

SNPshotrs121913088
SNPdbers121913088
MSV3drs121913088
GWAS Ctlgrs121913088
Max Magnitude0
OMIM134850
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121913088(A;A)
Alt rs121913088(A;A)
Reference rs121913088(G;G)
Significance Other
Disease FIBRINOGEN HAIFA 1
Variation info
Gene FGG
CLNDBN FIBRINOGEN HAIFA 1
Reversed 1
HGVS NC_000004.11:g.155528084C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017777.4,