rs786205674

Orientation

minus

Stabilized

minus

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

Make rs786205674(A;G)

Make rs786205674(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

65967798

Gene

GUSB

is a	snp
is	mentioned by
dbSNP	rs786205674
dbSNP (classic)	rs786205674
ClinGen	rs786205674
ebi	rs786205674
HLI	rs786205674
Exac	rs786205674
Gnomad	rs786205674
Varsome	rs786205674
LitVar	rs786205674
Map	rs786205674
PheGenI	rs786205674
Biobank	rs786205674
1000 genomes	rs786205674
hgdp	rs786205674
ensembl	rs786205674
geneview	rs786205674
scholar	rs786205674
google	rs786205674
pharmgkb	rs786205674
gwascentral	rs786205674
openSNP	rs786205674
23andMe	rs786205674
SNPshot	rs786205674
SNPdbe	rs786205674
MSV3d	rs786205674
GWAS Ctlg	rs786205674

Max Magnitude

0

ClinVar
Risk	rs786205674(G;G)
Alt	rs786205674(G;G)
Reference	Rs786205674(A;A)
Significance	Probable-Pathogenic
Disease	Non-immune hydrops fetalis
Variation	info
Gene	GUSB
CLNDBN	Non-immune hydrops fetalis
Reversed	1
HGVS	NC_000007.13:g.65432785T>C
CLNSRC
CLNACC	RCV000170585.1,