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rs587776839

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776839(A;A)
Make rs587776839(A;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position154608970
GeneFGG
is asnp
is mentioned by
dbSNPrs587776839
ebirs587776839
HLIrs587776839
Exacrs587776839
Varsomers587776839
Maprs587776839
PheGenIrs587776839
hapmaprs587776839
1000 genomesrs587776839
hgdprs587776839
ensemblrs587776839
gopubmedrs587776839
geneviewrs587776839
scholarrs587776839
googlers587776839
pharmgkbrs587776839
gwascentralrs587776839
openSNPrs587776839
23andMers587776839
23andMe allrs587776839
SNP Nexus

SNPshotrs587776839
SNPdbers587776839
MSV3drs587776839
GWAS Ctlgrs587776839
Max Magnitude0
ClinVar
Risk rs587776839(A;A)
Alt rs587776839(A;A)
Reference rs587776839(T;T)
Significance Pathogenic
Disease Afibrinogenemia
Variation info
Gene FGG
CLNDBN Afibrinogenemia, congenital
Reversed 0
HGVS NC_000004.11:g.155530122T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017802.28,