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rs606231224

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231224(G;T)
Make rs606231224(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position154569800
GeneFGB
is asnp
is mentioned by
dbSNPrs606231224
ebirs606231224
HLIrs606231224
Exacrs606231224
Varsomers606231224
Maprs606231224
PheGenIrs606231224
hapmaprs606231224
1000 genomesrs606231224
hgdprs606231224
ensemblrs606231224
gopubmedrs606231224
geneviewrs606231224
scholarrs606231224
googlers606231224
pharmgkbrs606231224
gwascentralrs606231224
openSNPrs606231224
23andMers606231224
23andMe allrs606231224
SNP Nexus

SNPshotrs606231224
SNPdbers606231224
MSV3drs606231224
GWAS Ctlgrs606231224
Max Magnitude0
ClinVar
Risk rs606231224(T;T)
Alt rs606231224(T;T)
Reference rs606231224(G;G)
Significance Pathogenic
Disease Afibrinogenemia
Variation info
Gene FGB
CLNDBN Afibrinogenemia, congenital
Reversed 0
HGVS NC_000004.11:g.155490952G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017819.27,