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rs606231223

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231223(C;T)
Make rs606231223(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position154569320
GeneFGB
is asnp
is mentioned by
dbSNPrs606231223
ebirs606231223
HLIrs606231223
Exacrs606231223
Varsomers606231223
Maprs606231223
PheGenIrs606231223
hapmaprs606231223
1000 genomesrs606231223
hgdprs606231223
ensemblrs606231223
gopubmedrs606231223
geneviewrs606231223
scholarrs606231223
googlers606231223
pharmgkbrs606231223
gwascentralrs606231223
openSNPrs606231223
23andMers606231223
23andMe allrs606231223
SNP Nexus

SNPshotrs606231223
SNPdbers606231223
MSV3drs606231223
GWAS Ctlgrs606231223
Max Magnitude0
ClinVar
Risk rs606231223(T;T)
Alt rs606231223(T;T)
Reference rs606231223(C;C)
Significance Pathogenic
Disease Afibrinogenemia
Variation info
Gene FGB
CLNDBN Afibrinogenemia, congenital
Reversed 0
HGVS NC_000004.11:g.155490472C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017818.27,