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rs61753266

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61753266(A;A)
Make rs61753266(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113140972
GeneF10
is asnp
is mentioned by
dbSNPrs61753266
ebirs61753266
HLIrs61753266
Exacrs61753266
Varsomers61753266
Maprs61753266
PheGenIrs61753266
hapmaprs61753266
1000 genomesrs61753266
hgdprs61753266
ensemblrs61753266
gopubmedrs61753266
geneviewrs61753266
scholarrs61753266
googlers61753266
pharmgkbrs61753266
gwascentralrs61753266
openSNPrs61753266
23andMers61753266
23andMe allrs61753266
SNP Nexus

SNPshotrs61753266
SNPdbers61753266
MSV3drs61753266
GWAS Ctlgrs61753266
GMAF0.0009183
Max Magnitude0
OMIM227600
Desc
Variant0007
Relatedalso
ClinVar
Risk rs61753266(A;A)
Alt rs61753266(A;A)
Reference rs61753266(G;G)
Significance Pathogenic
Disease Factor X deficiency
Variation info
Gene F10
CLNDBN Factor X deficiency
Reversed 0
HGVS NC_000013.10:g.113795286G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012841.4,