rs121964935

Orientation

plus

Stabilized

plus

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

Make rs121964935(A;A)

Make rs121964935(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

113110812

Gene

F7

is a	snp
is	mentioned by
dbSNP	rs121964935
dbSNP (classic)	rs121964935
ClinGen	rs121964935
ebi	rs121964935
HLI	rs121964935
Exac	rs121964935
Gnomad	rs121964935
Varsome	rs121964935
LitVar	rs121964935
Map	rs121964935
PheGenI	rs121964935
Biobank	rs121964935
1000 genomes	rs121964935
hgdp	rs121964935
ensembl	rs121964935
geneview	rs121964935
scholar	rs121964935
google	rs121964935
pharmgkb	rs121964935
gwascentral	rs121964935
openSNP	rs121964935
23andMe	rs121964935
SNPshot	rs121964935
SNPdbe	rs121964935
MSV3d	rs121964935
GWAS Ctlg	rs121964935

Max Magnitude

0

OMIM	227500
Desc
Variant	0021
Related	also

ClinVar
Risk	rs121964935(A;A)
Alt	rs121964935(A;A)
Reference	Rs121964935(G;G)
Significance	Probable-Pathogenic
Disease	Factor VII deficiency
Variation	info
Gene	F7
CLNDBN	Factor VII deficiency
Reversed	0
HGVS	NC_000013.10:g.113765126G>A
CLNSRC
CLNACC