rs104894392

Orientation

plus

Stabilized

plus

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

Make rs104894392(C;T)

Make rs104894392(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

113149146

Gene	F10, LOC102724474

is a	snp
is	mentioned by
dbSNP	rs104894392
dbSNP (classic)	rs104894392
ClinGen	rs104894392
ebi	rs104894392
HLI	rs104894392
Exac	rs104894392
Gnomad	rs104894392
Varsome	rs104894392
LitVar	rs104894392
Map	rs104894392
PheGenI	rs104894392
Biobank	rs104894392
1000 genomes	rs104894392
hgdp	rs104894392
ensembl	rs104894392
geneview	rs104894392
scholar	rs104894392
google	rs104894392
pharmgkb	rs104894392
gwascentral	rs104894392
openSNP	rs104894392
23andMe	rs104894392
SNPshot	rs104894392
SNPdbe	rs104894392
MSV3d	rs104894392
GWAS Ctlg	rs104894392

Max Magnitude

0

OMIM	227600
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894392(T;T)
Alt	rs104894392(T;T)
Reference	Rs104894392(C;C)
Significance	Pathogenic
Disease	Factor X deficiency
Variation	info
Gene	F10
CLNDBN	Factor X deficiency
Reversed	0
HGVS	NC_000013.10:g.113803460C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012833.4,