rs587783596

Orientation

plus

Stabilized

plus

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

Make rs587783596(A;G)

Make rs587783596(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

10812273

Gene

DNM2

is a	snp
is	mentioned by
dbSNP	rs587783596
dbSNP (classic)	rs587783596
ClinGen	rs587783596
ebi	rs587783596
HLI	rs587783596
Exac	rs587783596
Gnomad	rs587783596
Varsome	rs587783596
LitVar	rs587783596
Map	rs587783596
PheGenI	rs587783596
Biobank	rs587783596
1000 genomes	rs587783596
hgdp	rs587783596
ensembl	rs587783596
geneview	rs587783596
scholar	rs587783596
google	rs587783596
pharmgkb	rs587783596
gwascentral	rs587783596
openSNP	rs587783596
23andMe	rs587783596
SNPshot	rs587783596
SNPdbe	rs587783596
MSV3d	rs587783596
GWAS Ctlg	rs587783596

Max Magnitude

0

ClinVar
Risk	rs587783596(C;C) rs587783596(G;G)
Alt	rs587783596(C;C) rs587783596(G;G)
Reference	Rs587783596(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DNM2
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.10922949A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000145904.1,