rs1801202

Orientation

plus

Stabilized

plus

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

Make rs1801202(C;T)

Make rs1801202(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139561592

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs1801202
dbSNP (classic)	rs1801202
ClinGen	rs1801202
ebi	rs1801202
HLI	rs1801202
Exac	rs1801202
Gnomad	rs1801202
Varsome	rs1801202
LitVar	rs1801202
Map	rs1801202
PheGenI	rs1801202
Biobank	rs1801202
1000 genomes	rs1801202
hgdp	rs1801202
ensembl	rs1801202
geneview	rs1801202
scholar	rs1801202
google	rs1801202
pharmgkb	rs1801202
gwascentral	rs1801202
openSNP	rs1801202
23andMe	rs1801202
SNPshot	rs1801202
SNPdbe	rs1801202
MSV3d	rs1801202
GWAS Ctlg	rs1801202

Max Magnitude

0

OMIM	300746
Desc
Variant	0085
Related	also

ClinVar
Risk	rs1801202(T;T)
Alt	rs1801202(T;T)
Reference	Rs1801202(C;C)
Significance	Non-pathogenic
Disease	FACTOR IX POLYMORPHISM
Variation	info
Gene	F9
CLNDBN	FACTOR IX POLYMORPHISM
Reversed	0
HGVS	NC_000023.10:g.138643751C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011387.1,