rs879254086

Orientation

plus

Stabilized

plus

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

Make rs879254086(A;A)

Make rs879254086(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

19

Position

10819986

Gene

DNM2

is a	snp
is	mentioned by
dbSNP	rs879254086
dbSNP (classic)	rs879254086
ClinGen	rs879254086
ebi	rs879254086
HLI	rs879254086
Exac	rs879254086
Gnomad	rs879254086
Varsome	rs879254086
LitVar	rs879254086
Map	rs879254086
PheGenI	rs879254086
Biobank	rs879254086
1000 genomes	rs879254086
hgdp	rs879254086
ensembl	rs879254086
geneview	rs879254086
scholar	rs879254086
google	rs879254086
pharmgkb	rs879254086
gwascentral	rs879254086
openSNP	rs879254086
23andMe	rs879254086
SNPshot	rs879254086
SNPdbe	rs879254086
MSV3d	rs879254086
GWAS Ctlg	rs879254086

Max Magnitude

0

ClinVar
Risk	rs879254086(A;A)
Alt	rs879254086(A;A)
Reference	Rs879254086(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DNM2
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.10930662G>A
CLNSRC
CLNACC	RCV000236107.1,