rs1800578

Orientation

minus

Stabilized

minus

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

Make rs1800578(C;T)

Make rs1800578(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

23048022

Gene

THBD

is a	snp
is	mentioned by
dbSNP	rs1800578
dbSNP (classic)	rs1800578
ClinGen	rs1800578
ebi	rs1800578
HLI	rs1800578
Exac	rs1800578
Gnomad	rs1800578
Varsome	rs1800578
LitVar	rs1800578
Map	rs1800578
PheGenI	rs1800578
Biobank	rs1800578
1000 genomes	rs1800578
hgdp	rs1800578
ensembl	rs1800578
geneview	rs1800578
scholar	rs1800578
google	rs1800578
pharmgkb	rs1800578
gwascentral	rs1800578
openSNP	rs1800578
23andMe	rs1800578
SNPshot	rs1800578
SNPdbe	rs1800578
MSV3d	rs1800578
GWAS Ctlg	rs1800578

Max Magnitude

0

OMIM	188040
Desc
Variant	0007
Related	also

ClinVar
Risk	rs1800578(A;A) rs1800578(T;T)
Alt	rs1800578(A;A) rs1800578(T;T)
Reference	Rs1800578(C;C)
Significance	Other
Disease	Atypical hemolytic-uremic syndrome 6
Variation	info
Gene	THBD
CLNDBN	Atypical hemolytic-uremic syndrome 6
Reversed	1
HGVS	NC_000020.10:g.23028659G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013557.2,

[PMID 17677000] Combined effects of thrombosis pathway gene variants predict cardiovascular events.