rs121964931

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121964931(C;T)

Make rs121964931(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

113118518

Gene

F7

is a	snp
is	mentioned by
dbSNP	rs121964931
dbSNP (classic)	rs121964931
ClinGen	rs121964931
ebi	rs121964931
HLI	rs121964931
Exac	rs121964931
Gnomad	rs121964931
Varsome	rs121964931
LitVar	rs121964931
Map	rs121964931
PheGenI	rs121964931
Biobank	rs121964931
1000 genomes	rs121964931
hgdp	rs121964931
ensembl	rs121964931
geneview	rs121964931
scholar	rs121964931
google	rs121964931
pharmgkb	rs121964931
gwascentral	rs121964931
openSNP	rs121964931
23andMe	rs121964931
SNPshot	rs121964931
SNPdbe	rs121964931
MSV3d	rs121964931
GWAS Ctlg	rs121964931

Max Magnitude

0

OMIM	227500
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121964931(T;T)
Alt	rs121964931(T;T)
Reference	Rs121964931(C;C)
Significance	Probable-Pathogenic
Disease	Factor VII deficiency
Variation	info
Gene	F7
CLNDBN	Factor VII deficiency
Reversed	0
HGVS	NC_000013.10:g.113772832C>T
CLNSRC
CLNACC