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rs587776837

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776837(C;T)
Make rs587776837(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position154612527
GeneFGG
is asnp
is mentioned by
dbSNPrs587776837
ebirs587776837
HLIrs587776837
Exacrs587776837
Varsomers587776837
Maprs587776837
PheGenIrs587776837
hapmaprs587776837
1000 genomesrs587776837
hgdprs587776837
ensemblrs587776837
gopubmedrs587776837
geneviewrs587776837
scholarrs587776837
googlers587776837
pharmgkbrs587776837
gwascentralrs587776837
openSNPrs587776837
23andMers587776837
23andMe allrs587776837
SNP Nexus

SNPshotrs587776837
SNPdbers587776837
MSV3drs587776837
GWAS Ctlgrs587776837
Max Magnitude0
ClinVar
Risk rs587776837(T;T)
Alt rs587776837(T;T)
Reference rs587776837(C;C)
Significance Pathogenic
Disease Afibrinogenemia
Variation info
Gene FGG
CLNDBN Afibrinogenemia, congenital
Reversed 0
HGVS NC_000004.11:g.155533679C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017798.24,