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rs786205091

From SNPedia

Orientationplus
Geno Mag Summary
(GCGGGTGGCGCAGGTCA;GCGGGTGGCGCAGGTCA) 0 common in clinvar
Make rs786205091(-;-)
Make rs786205091(-;GCGGGTGGCGCAGGTCA)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position113118456
GeneF7
is asnp
is mentioned by
dbSNPrs786205091
ebirs786205091
HLIrs786205091
Exacrs786205091
Varsomers786205091
Maprs786205091
PheGenIrs786205091
hapmaprs786205091
1000 genomesrs786205091
hgdprs786205091
ensemblrs786205091
gopubmedrs786205091
geneviewrs786205091
scholarrs786205091
googlers786205091
pharmgkbrs786205091
gwascentralrs786205091
openSNPrs786205091
23andMers786205091
23andMe allrs786205091
SNP Nexus

SNPshotrs786205091
SNPdbers786205091
MSV3drs786205091
GWAS Ctlgrs786205091
Max Magnitude0
ClinVar
Risk rs786205091(;)
Alt rs786205091(;)
Reference rs786205091(GCGGGTGGCGCAGGTCA;GCGGGTGGCGCAGGTCA)
Significance Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113772770_113772786del17
CLNSRC OMIM Allelic Variant
CLNACC RCV000012858.4,