rs786205669

Orientation

minus

Stabilized

minus

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

Make rs786205669(A;A)

Make rs786205669(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

52397636

Gene

THSD1

is a	snp
is	mentioned by
dbSNP	rs786205669
dbSNP (classic)	rs786205669
ClinGen	rs786205669
ebi	rs786205669
HLI	rs786205669
Exac	rs786205669
Gnomad	rs786205669
Varsome	rs786205669
LitVar	rs786205669
Map	rs786205669
PheGenI	rs786205669
Biobank	rs786205669
1000 genomes	rs786205669
hgdp	rs786205669
ensembl	rs786205669
geneview	rs786205669
scholar	rs786205669
google	rs786205669
pharmgkb	rs786205669
gwascentral	rs786205669
openSNP	rs786205669
23andMe	rs786205669
SNPshot	rs786205669
SNPdbe	rs786205669
MSV3d	rs786205669
GWAS Ctlg	rs786205669

Max Magnitude

0

ClinVar
Risk	rs786205669(A;A)
Alt	rs786205669(A;A)
Reference	Rs786205669(G;G)
Significance	Probable-Pathogenic
Disease	Non-immune hydrops fetalis
Variation	info
Gene	THSD1
CLNDBN	Non-immune hydrops fetalis
Reversed	1
HGVS	NC_000013.10:g.52971771C>T
CLNSRC
CLNACC	RCV000170576.1,