rs137852236

Orientation

plus

Stabilized

plus

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

Make rs137852236(A;T)

Make rs137852236(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139548467

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852236
dbSNP (classic)	rs137852236
ClinGen	rs137852236
ebi	rs137852236
HLI	rs137852236
Exac	rs137852236
Gnomad	rs137852236
Varsome	rs137852236
LitVar	rs137852236
Map	rs137852236
PheGenI	rs137852236
Biobank	rs137852236
1000 genomes	rs137852236
hgdp	rs137852236
ensembl	rs137852236
geneview	rs137852236
scholar	rs137852236
google	rs137852236
pharmgkb	rs137852236
gwascentral	rs137852236
openSNP	rs137852236
23andMe	rs137852236
SNPshot	rs137852236
SNPdbe	rs137852236
MSV3d	rs137852236
GWAS Ctlg	rs137852236

Max Magnitude

0

OMIM	300746
Desc
Variant	0025
Related	also

ClinVar
Risk	rs137852236(G;G) rs137852236(T;T)
Alt	rs137852236(G;G) rs137852236(T;T)
Reference	Rs137852236(A;A)
Significance	Pathogenic
Disease	Hereditary factor IX deficiency disease
Variation	info
Gene	F9
CLNDBN	Hereditary factor IX deficiency disease
Reversed	0
HGVS	NC_000023.10:g.138630626A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011328.7,