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

rs121965062

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121965062(A;A)
Make rs121965062(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position1754289
GeneSERPINF2
is asnp
is mentioned by
dbSNPrs121965062
ebirs121965062
HLIrs121965062
Exacrs121965062
Varsomers121965062
Maprs121965062
PheGenIrs121965062
hapmaprs121965062
1000 genomesrs121965062
hgdprs121965062
ensemblrs121965062
gopubmedrs121965062
geneviewrs121965062
scholarrs121965062
googlers121965062
pharmgkbrs121965062
gwascentralrs121965062
openSNPrs121965062
23andMers121965062
23andMe allrs121965062
SNP Nexus

SNPshotrs121965062
SNPdbers121965062
MSV3drs121965062
GWAS Ctlgrs121965062
Max Magnitude0
OMIM613168
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121965062(A;A)
Alt rs121965062(A;A)
Reference rs121965062(G;G)
Significance Pathogenic
Disease Anti-plasmin deficiency
Variation info
Gene SERPINF2
CLNDBN Anti-plasmin deficiency, congenital
Reversed 0
HGVS NC_000017.10:g.1657583G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000300.2,