rs121909094

Orientation

plus

Stabilized

plus

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

Make rs121909094(A;A)

Make rs121909094(A;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

10820017

Gene

DNM2

is a	snp
is	mentioned by
dbSNP	rs121909094
dbSNP (classic)	rs121909094
ClinGen	rs121909094
ebi	rs121909094
HLI	rs121909094
Exac	rs121909094
Gnomad	rs121909094
Varsome	rs121909094
LitVar	rs121909094
Map	rs121909094
PheGenI	rs121909094
Biobank	rs121909094
1000 genomes	rs121909094
hgdp	rs121909094
ensembl	rs121909094
geneview	rs121909094
scholar	rs121909094
google	rs121909094
pharmgkb	rs121909094
gwascentral	rs121909094
openSNP	rs121909094
23andMe	rs121909094
SNPshot	rs121909094
SNPdbe	rs121909094
MSV3d	rs121909094
GWAS Ctlg	rs121909094

Max Magnitude

0

OMIM	602378
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121909094(A;A)
Alt	rs121909094(A;A)
Reference	Rs121909094(T;T)
Significance	Pathogenic
Disease	Charcot-Marie-Tooth disease
Variation	info
Gene	DNM2
CLNDBN	Charcot-Marie-Tooth disease, type 2M
Reversed	0
HGVS	NC_000019.9:g.10930693T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007707.3,