rs1057521074

Orientation

minus

Stabilized

minus

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

Make rs1057521074(A;A)

Make rs1057521074(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

154902063

Gene

F8

is a	snp
is	mentioned by
dbSNP	rs1057521074
dbSNP (classic)	rs1057521074
ClinGen	rs1057521074
ebi	rs1057521074
HLI	rs1057521074
Exac	rs1057521074
Gnomad	rs1057521074
Varsome	rs1057521074
LitVar	rs1057521074
Map	rs1057521074
PheGenI	rs1057521074
Biobank	rs1057521074
1000 genomes	rs1057521074
hgdp	rs1057521074
ensembl	rs1057521074
geneview	rs1057521074
scholar	rs1057521074
google	rs1057521074
pharmgkb	rs1057521074
gwascentral	rs1057521074
openSNP	rs1057521074
23andMe	rs1057521074
SNPshot	rs1057521074
SNPdbe	rs1057521074
MSV3d	rs1057521074
GWAS Ctlg	rs1057521074

Max Magnitude

0

ClinVar
Risk	rs1057521074(A;A)
Alt	rs1057521074(A;A)
Reference	Rs1057521074(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	F8
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.154130338C>T
CLNSRC
CLNACC	RCV000442362.1,