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rs267606790

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606790(C;T)
Make rs267606790(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113116822
GeneF7
is asnp
is mentioned by
dbSNPrs267606790
ebirs267606790
HLIrs267606790
Exacrs267606790
Varsomers267606790
Maprs267606790
PheGenIrs267606790
hapmaprs267606790
1000 genomesrs267606790
hgdprs267606790
ensemblrs267606790
gopubmedrs267606790
geneviewrs267606790
scholarrs267606790
googlers267606790
pharmgkbrs267606790
gwascentralrs267606790
openSNPrs267606790
23andMers267606790
23andMe allrs267606790
SNP Nexus

SNPshotrs267606790
SNPdbers267606790
MSV3drs267606790
GWAS Ctlgrs267606790
Max Magnitude0
ClinVar
Risk rs267606790(T;T)
Alt rs267606790(T;T)
Reference rs267606790(C;C)
Significance Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113771136C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012867.3,