rs794728981

Orientation

plus

Stabilized

plus

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

Make rs794728981(-;-)

Make rs794728981(-;CTGAAAGTGG)

Make rs794728981(CTGAAAGTGG;CTGAAAGTGG)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

119676821

Gene

BAG3

is a	snp
is	mentioned by
dbSNP	rs794728981
dbSNP (classic)	rs794728981
ClinGen	rs794728981
ebi	rs794728981
HLI	rs794728981
Exac	rs794728981
Gnomad	rs794728981
Varsome	rs794728981
LitVar	rs794728981
Map	rs794728981
PheGenI	rs794728981
Biobank	rs794728981
1000 genomes	rs794728981
hgdp	rs794728981
ensembl	rs794728981
geneview	rs794728981
scholar	rs794728981
google	rs794728981
pharmgkb	rs794728981
gwascentral	rs794728981
openSNP	rs794728981
23andMe	rs794728981
SNPshot	rs794728981
SNPdbe	rs794728981
MSV3d	rs794728981
GWAS Ctlg	rs794728981

Max Magnitude

0

ClinVar
Risk	rs794728981(-;-)
Alt	rs794728981(-;-)
Reference	Rs794728981(GCTGAAAGTG;GCTGAAAGTG)
Significance	Pathogenic
Disease	not provided Inborn genetic diseases
Variation	info
Gene	BAG3
CLNDBN	not provided Inborn genetic diseases
Reversed	0
HGVS	NC_000010.10:g.121436333_121436342delCTGAAAGTGG
CLNSRC
CLNACC	RCV000183323.1, RCV000190668.1,