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

rs587776838

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776838(C;T)
Make rs587776838(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position154612013
GeneFGG
is asnp
is mentioned by
dbSNPrs587776838
ebirs587776838
HLIrs587776838
Exacrs587776838
Varsomers587776838
Maprs587776838
PheGenIrs587776838
hapmaprs587776838
1000 genomesrs587776838
hgdprs587776838
ensemblrs587776838
gopubmedrs587776838
geneviewrs587776838
scholarrs587776838
googlers587776838
pharmgkbrs587776838
gwascentralrs587776838
openSNPrs587776838
23andMers587776838
23andMe allrs587776838
SNP Nexus

SNPshotrs587776838
SNPdbers587776838
MSV3drs587776838
GWAS Ctlgrs587776838
Max Magnitude0
ClinVar
Risk rs587776838(T;T)
Alt rs587776838(T;T)
Reference rs587776838(C;C)
Significance Pathogenic
Disease Afibrinogenemia
Variation info
Gene FGG
CLNDBN Afibrinogenemia, congenital
Reversed 0
HGVS NC_000004.11:g.155533165C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017799.28,