rs121964948

Orientation

plus

Stabilized

plus

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

Make rs121964948(A;T)

Make rs121964948(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

113147490

Gene

F10

is a	snp
is	mentioned by
dbSNP	rs121964948
dbSNP (classic)	rs121964948
ClinGen	rs121964948
ebi	rs121964948
HLI	rs121964948
Exac	rs121964948
Gnomad	rs121964948
Varsome	rs121964948
LitVar	rs121964948
Map	rs121964948
PheGenI	rs121964948
Biobank	rs121964948
1000 genomes	rs121964948
hgdp	rs121964948
ensembl	rs121964948
geneview	rs121964948
scholar	rs121964948
google	rs121964948
pharmgkb	rs121964948
gwascentral	rs121964948
openSNP	rs121964948
23andMe	rs121964948
SNPshot	rs121964948
SNPdbe	rs121964948
MSV3d	rs121964948
GWAS Ctlg	rs121964948

Max Magnitude

0

OMIM	227600
Desc
Variant	0014
Related	also

ClinVar
Risk	rs121964948(T;T)
Alt	rs121964948(T;T)
Reference	Rs121964948(A;A)
Significance	Pathogenic
Disease	Factor X deficiency
Variation	info
Gene	F10
CLNDBN	Factor X deficiency
Reversed	0
HGVS	NC_000013.10:g.113801804A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012839.3,