rs387906508

Orientation

plus

Stabilized

plus

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

Make rs387906508(C;C)

Make rs387906508(C;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

113118590

Gene

F7

is a	snp
is	mentioned by
dbSNP	rs387906508
dbSNP (classic)	rs387906508
ClinGen	rs387906508
ebi	rs387906508
HLI	rs387906508
Exac	rs387906508
Gnomad	rs387906508
Varsome	rs387906508
LitVar	rs387906508
Map	rs387906508
PheGenI	rs387906508
Biobank	rs387906508
1000 genomes	rs387906508
hgdp	rs387906508
ensembl	rs387906508
geneview	rs387906508
scholar	rs387906508
google	rs387906508
pharmgkb	rs387906508
gwascentral	rs387906508
openSNP	rs387906508
23andMe	rs387906508
SNPshot	rs387906508
SNPdbe	rs387906508
MSV3d	rs387906508
GWAS Ctlg	rs387906508

Max Magnitude

0

ClinVar
Risk	rs387906508(C;C)
Alt	rs387906508(C;C)
Reference	Rs387906508(T;T)
Significance	Pathogenic
Disease	Factor VII deficiency
Variation	info
Gene	F7
CLNDBN	Factor VII deficiency
Reversed	0
HGVS	NC_000013.10:g.113772904T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012871.3,