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rs606231225

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs606231225(-;-)
Make rs606231225(-;T)
Make rs606231225(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position154586717
GeneFGA
is asnp
is mentioned by
dbSNPrs606231225
ebirs606231225
HLIrs606231225
Exacrs606231225
Varsomers606231225
Maprs606231225
PheGenIrs606231225
hapmaprs606231225
1000 genomesrs606231225
hgdprs606231225
ensemblrs606231225
gopubmedrs606231225
geneviewrs606231225
scholarrs606231225
googlers606231225
pharmgkbrs606231225
gwascentralrs606231225
openSNPrs606231225
23andMers606231225
23andMe allrs606231225
SNP Nexus

SNPshotrs606231225
SNPdbers606231225
MSV3drs606231225
GWAS Ctlgrs606231225
Max Magnitude0
ClinVar
Risk rs606231225(T;T)
Alt rs606231225(T;T)
Reference rs606231225(;)
Significance Pathogenic
Disease Afibrinogenemia
Variation info
Gene FGA
CLNDBN Afibrinogenemia, congenital
Reversed 1
HGVS NC_000004.11:g.155507870dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000017879.23,