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rs36209567

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs36209567(C;T)
Make rs36209567(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113118668
GeneF7
is asnp
is mentioned by
dbSNPrs36209567
ebirs36209567
HLIrs36209567
Exacrs36209567
Varsomers36209567
Maprs36209567
PheGenIrs36209567
hapmaprs36209567
1000 genomesrs36209567
hgdprs36209567
ensemblrs36209567
gopubmedrs36209567
geneviewrs36209567
scholarrs36209567
googlers36209567
pharmgkbrs36209567
gwascentralrs36209567
openSNPrs36209567
23andMers36209567
23andMe allrs36209567
SNP Nexus

SNPshotrs36209567
SNPdbers36209567
MSV3drs36209567
GWAS Ctlgrs36209567
GMAF0.0009183
Max Magnitude0
OMIM227500
Desc
Variant0010
Relatedalso
ClinVar
Risk rs36209567(T;T)
Alt rs36209567(T;T)
Reference rs36209567(C;C)
Significance Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113772982C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012857.3,