Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909607

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909607(A;A)
Make rs121909607(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154589513
GeneFGA
is asnp
is mentioned by
dbSNPrs121909607
ebirs121909607
HLIrs121909607
Exacrs121909607
Varsomers121909607
Maprs121909607
PheGenIrs121909607
hapmaprs121909607
1000 genomesrs121909607
hgdprs121909607
ensemblrs121909607
gopubmedrs121909607
geneviewrs121909607
scholarrs121909607
googlers121909607
pharmgkbrs121909607
gwascentralrs121909607
openSNPrs121909607
23andMers121909607
23andMe allrs121909607
SNP Nexus

SNPshotrs121909607
SNPdbers121909607
MSV3drs121909607
GWAS Ctlgrs121909607
Max Magnitude0
OMIM134820
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909607(A;A)
Alt rs121909607(A;A)
Reference rs121909607(G;G)
Significance Pathogenic
Disease Dysfibrinogenemia
Variation info
Gene FGA
CLNDBN Dysfibrinogenemia
Reversed 1
HGVS NC_000004.11:g.155510665C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030941.7,