rs121913072

Orientation

minus

Stabilized

minus

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

Make rs121913072(A;A)

Make rs121913072(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

6222165

Gene

F13A1

is a	snp
is	mentioned by
dbSNP	rs121913072
dbSNP (classic)	rs121913072
ClinGen	rs121913072
ebi	rs121913072
HLI	rs121913072
Exac	rs121913072
Gnomad	rs121913072
Varsome	rs121913072
LitVar	rs121913072
Map	rs121913072
PheGenI	rs121913072
Biobank	rs121913072
1000 genomes	rs121913072
hgdp	rs121913072
ensembl	rs121913072
geneview	rs121913072
scholar	rs121913072
google	rs121913072
pharmgkb	rs121913072
gwascentral	rs121913072
openSNP	rs121913072
23andMe	rs121913072
SNPshot	rs121913072
SNPdbe	rs121913072
MSV3d	rs121913072
GWAS Ctlg	rs121913072

Max Magnitude

0

OMIM	134570
Desc
Variant	0011
Related	also

ClinVar
Risk	rs121913072(A;A)
Alt	rs121913072(A;A)
Reference	Rs121913072(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.6222398C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017998.24,