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rs61754487

From SNPedia

Orientationplus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(G;G) 0
Make rs61754487(A;A)
Make rs61754487(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position94288306
GeneSERPINA10
is asnp
is mentioned by
dbSNPrs61754487
ebirs61754487
HLIrs61754487
Exacrs61754487
Varsomers61754487
Maprs61754487
PheGenIrs61754487
hapmaprs61754487
1000 genomesrs61754487
hgdprs61754487
ensemblrs61754487
gopubmedrs61754487
geneviewrs61754487
scholarrs61754487
googlers61754487
pharmgkbrs61754487
gwascentralrs61754487
openSNPrs61754487
23andMers61754487
23andMe allrs61754487
SNP Nexus

SNPshotrs61754487
SNPdbers61754487
MSV3drs61754487
GWAS Ctlgrs61754487
GMAF0.002296
Max Magnitude0
OMIM605271
Desc
Variant0001
Relatedalso


ClinVar
Risk rs61754487(T;T)
Alt rs61754487(T;T)
Reference rs61754487(C;C)
Significance Other
Disease Venous thrombosis
Variation info
Gene SERPINA10
CLNDBN Venous thrombosis, susceptibility to
Reversed 0
HGVS NC_000014.8:g.94754643C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005413.3,