rs118203889

Orientation

plus

Stabilized

plus

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

Make rs118203889(A;A)

Make rs118203889(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

12207

is a	snp
is	mentioned by
dbSNP	rs118203889
dbSNP (classic)	rs118203889
ClinGen	rs118203889
ebi	rs118203889
HLI	rs118203889
Exac	rs118203889
Gnomad	rs118203889
Varsome	rs118203889
LitVar	rs118203889
Map	rs118203889
PheGenI	rs118203889
Biobank	rs118203889
1000 genomes	rs118203889
hgdp	rs118203889
ensembl	rs118203889
geneview	rs118203889
scholar	rs118203889
google	rs118203889
pharmgkb	rs118203889
gwascentral	rs118203889
openSNP	rs118203889
23andMe	rs118203889
SNPshot	rs118203889
SNPdbe	rs118203889
MSV3d	rs118203889
GWAS Ctlg	rs118203889

Max Magnitude

0

ClinVar
Risk	rs118203889(A;A)
Alt	rs118203889(A;A)
Reference	Rs118203889(G;G)
Significance	Pathogenic
Disease	MERRF/MELAS overlap syndrome
Variation	info
Gene
CLNDBN	MERRF/MELAS overlap syndrome
Reversed	0
HGVS	NC_012920.1:m.12207G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010173.2,