rs121913070

Orientation

minus

Stabilized

minus

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

Make rs121913070(G;T)

Make rs121913070(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

6195859

Gene

F13A1

is a	snp
is	mentioned by
dbSNP	rs121913070
dbSNP (classic)	rs121913070
ClinGen	rs121913070
ebi	rs121913070
HLI	rs121913070
Exac	rs121913070
Gnomad	rs121913070
Varsome	rs121913070
LitVar	rs121913070
Map	rs121913070
PheGenI	rs121913070
Biobank	rs121913070
1000 genomes	rs121913070
hgdp	rs121913070
ensembl	rs121913070
geneview	rs121913070
scholar	rs121913070
google	rs121913070
pharmgkb	rs121913070
gwascentral	rs121913070
openSNP	rs121913070
23andMe	rs121913070
SNPshot	rs121913070
SNPdbe	rs121913070
MSV3d	rs121913070
GWAS Ctlg	rs121913070

Max Magnitude

0

OMIM	134570
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121913070(T;T)
Alt	rs121913070(T;T)
Reference	Rs121913070(G;G)
Significance	Pathogenic
Disease	Factor xiii
Variation	info
Gene	F13A1
CLNDBN	Factor xiii, a subunit, deficiency of
Reversed	1
HGVS	NC_000006.11:g.6196092C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017994.24,