rs886039704

Orientation

plus

Stabilized

plus

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

Make rs886039704(C;G)

Make rs886039704(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

19

Position

10823885

Gene

DNM2

is a	snp
is	mentioned by
dbSNP	rs886039704
dbSNP (classic)	rs886039704
ClinGen	rs886039704
ebi	rs886039704
HLI	rs886039704
Exac	rs886039704
Gnomad	rs886039704
Varsome	rs886039704
LitVar	rs886039704
Map	rs886039704
PheGenI	rs886039704
Biobank	rs886039704
1000 genomes	rs886039704
hgdp	rs886039704
ensembl	rs886039704
geneview	rs886039704
scholar	rs886039704
google	rs886039704
pharmgkb	rs886039704
gwascentral	rs886039704
openSNP	rs886039704
23andMe	rs886039704
SNPshot	rs886039704
SNPdbe	rs886039704
MSV3d	rs886039704
GWAS Ctlg	rs886039704

Max Magnitude

0

ClinVar
Risk	rs886039704(G;G)
Alt	rs886039704(G;G)
Reference	Rs886039704(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DNM2
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.10934561C>G
CLNSRC
CLNACC	RCV000255790.1,