rs121913068

Orientation

minus

Stabilized

minus

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

Make rs121913068(A;A)

Make rs121913068(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

6174823

Gene

F13A1

is a	snp
is	mentioned by
dbSNP	rs121913068
dbSNP (classic)	rs121913068
ClinGen	rs121913068
ebi	rs121913068
HLI	rs121913068
Exac	rs121913068
Gnomad	rs121913068
Varsome	rs121913068
LitVar	rs121913068
Map	rs121913068
PheGenI	rs121913068
Biobank	rs121913068
1000 genomes	rs121913068
hgdp	rs121913068
ensembl	rs121913068
geneview	rs121913068
scholar	rs121913068
google	rs121913068
pharmgkb	rs121913068
gwascentral	rs121913068
openSNP	rs121913068
23andMe	rs121913068
SNPshot	rs121913068
SNPdbe	rs121913068
MSV3d	rs121913068
GWAS Ctlg	rs121913068

Max Magnitude

0

OMIM	134570
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121913068(A;A)
Alt	rs121913068(A;A)
Reference	Rs121913068(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.6175056C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017992.28,