rs121913064

Orientation

minus

Stabilized

minus

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

Make rs121913064(A;A)

Make rs121913064(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

6151813

Gene

F13A1

is a	snp
is	mentioned by
dbSNP	rs121913064
dbSNP (classic)	rs121913064
ClinGen	rs121913064
ebi	rs121913064
HLI	rs121913064
Exac	rs121913064
Gnomad	rs121913064
Varsome	rs121913064
LitVar	rs121913064
Map	rs121913064
PheGenI	rs121913064
Biobank	rs121913064
1000 genomes	rs121913064
hgdp	rs121913064
ensembl	rs121913064
geneview	rs121913064
scholar	rs121913064
google	rs121913064
pharmgkb	rs121913064
gwascentral	rs121913064
openSNP	rs121913064
23andMe	rs121913064
SNPshot	rs121913064
SNPdbe	rs121913064
MSV3d	rs121913064
GWAS Ctlg	rs121913064

Max Magnitude

0

OMIM	134570
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121913064(A;A) rs121913064(T;T)
Alt	rs121913064(A;A) rs121913064(T;T)
Reference	Rs121913064(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.6152046C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017988.27,