rs5987

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs5987(A;A)

Make rs5987(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

6151907

Gene

F13A1

is a	snp
is	mentioned by
dbSNP	rs5987
dbSNP (classic)	rs5987
ClinGen	rs5987
ebi	rs5987
HLI	rs5987
Exac	rs5987
Gnomad	rs5987
Varsome	rs5987
LitVar	rs5987
Map	rs5987
PheGenI	rs5987
Biobank	rs5987
1000 genomes	rs5987
hgdp	rs5987
ensembl	rs5987
geneview	rs5987
scholar	rs5987
google	rs5987
pharmgkb	rs5987
gwascentral	rs5987
openSNP	rs5987
23andMe	rs5987
SNPshot	rs5987
SNPdbe	rs5987
MSV3d	rs5987
GWAS Ctlg	rs5987

GMAF

0.06749

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	rs5987(A;A)
Alt	rs5987(A;A)
Reference	Rs5987(G;G)
Significance	Probable-non-pathogenic
Disease	not specified Factor xiii
Variation	info
Gene	F13A1
CLNDBN	not specified Factor xiii, a subunit, deficiency of
Reversed	1
HGVS	NC_000006.11:g.6152140C>T
CLNSRC
CLNACC	RCV000252406.1, RCV000297230.1,