rs118203886

Orientation

plus

Stabilized

plus

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

Make rs118203886(A;A)

Make rs118203886(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

611

is a	snp
is	mentioned by
dbSNP	rs118203886
dbSNP (classic)	rs118203886
ClinGen	rs118203886
ebi	rs118203886
HLI	rs118203886
Exac	rs118203886
Gnomad	rs118203886
Varsome	rs118203886
LitVar	rs118203886
Map	rs118203886
PheGenI	rs118203886
Biobank	rs118203886
1000 genomes	rs118203886
hgdp	rs118203886
ensembl	rs118203886
geneview	rs118203886
scholar	rs118203886
google	rs118203886
pharmgkb	rs118203886
gwascentral	rs118203886
openSNP	rs118203886
23andMe	rs118203886
SNPshot	rs118203886
SNPdbe	rs118203886
MSV3d	rs118203886
GWAS Ctlg	rs118203886

Max Magnitude

0

ClinVar
Risk	rs118203886(A;A)
Alt	rs118203886(A;A)
Reference	Rs118203886(G;G)
Significance	Pathogenic
Disease	Myoclonus with epilepsy with ragged red fibers
Variation	info
Gene
CLNDBN	Myoclonus with epilepsy with ragged red fibers
Reversed	0
HGVS	NC_012920.1:m.611G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010187.5,