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

rs587777720

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777720(A;G)
Make rs587777720(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position154604986
GeneFGG
is asnp
is mentioned by
dbSNPrs587777720
ebirs587777720
HLIrs587777720
Exacrs587777720
Varsomers587777720
Maprs587777720
PheGenIrs587777720
hapmaprs587777720
1000 genomesrs587777720
hgdprs587777720
ensemblrs587777720
gopubmedrs587777720
geneviewrs587777720
scholarrs587777720
googlers587777720
pharmgkbrs587777720
gwascentralrs587777720
openSNPrs587777720
23andMers587777720
23andMe allrs587777720
SNP Nexus

SNPshotrs587777720
SNPdbers587777720
MSV3drs587777720
GWAS Ctlgrs587777720
Max Magnitude0
ClinVar
Risk rs587777720(G;G)
Alt rs587777720(G;G)
Reference rs587777720(A;A)
Significance Pathogenic
Disease Hypodysfibrinogenemia
Variation info
Gene FGG
CLNDBN Hypodysfibrinogenemia
Reversed 0
HGVS NC_000004.11:g.155526138A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000144152.3,