rs886039325

Orientation

plus

Stabilized

plus

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

Make rs886039325(C;C)

Make rs886039325(C;G)

Reference

GRCh38.p7 38.3/149

Chromosome

3

Position

8745714

Gene	CAV3, SSUH2

is a	snp
is	mentioned by
dbSNP	rs886039325
dbSNP (classic)	rs886039325
ClinGen	rs886039325
ebi	rs886039325
HLI	rs886039325
Exac	rs886039325
Gnomad	rs886039325
Varsome	rs886039325
LitVar	rs886039325
Map	rs886039325
PheGenI	rs886039325
Biobank	rs886039325
1000 genomes	rs886039325
hgdp	rs886039325
ensembl	rs886039325
geneview	rs886039325
scholar	rs886039325
google	rs886039325
pharmgkb	rs886039325
gwascentral	rs886039325
openSNP	rs886039325
23andMe	rs886039325
SNPshot	rs886039325
SNPdbe	rs886039325
MSV3d	rs886039325
GWAS Ctlg	rs886039325

Max Magnitude

0

ClinVar
Risk	rs886039325(C;C)
Alt	rs886039325(C;C)
Reference	Rs886039325(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SSUH2 CAV3
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.8787400G>C
CLNSRC
CLNACC	RCV000256116.1,