rs199474661

Orientation

plus

Stabilized

plus

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

Make rs199474661(A;G)

Make rs199474661(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

3252

is a	snp
is	mentioned by
dbSNP	rs199474661
dbSNP (classic)	rs199474661
ClinGen	rs199474661
ebi	rs199474661
HLI	rs199474661
Exac	rs199474661
Gnomad	rs199474661
Varsome	rs199474661
LitVar	rs199474661
Map	rs199474661
PheGenI	rs199474661
Biobank	rs199474661
1000 genomes	rs199474661
hgdp	rs199474661
ensembl	rs199474661
geneview	rs199474661
scholar	rs199474661
google	rs199474661
pharmgkb	rs199474661
gwascentral	rs199474661
openSNP	rs199474661
23andMe	rs199474661
SNPshot	rs199474661
SNPdbe	rs199474661
MSV3d	rs199474661
GWAS Ctlg	rs199474661

Max Magnitude

0

ClinVar
Risk	rs199474661(G;G)
Alt	rs199474661(G;G)
Reference	Rs199474661(A;A)
Significance	Pathogenic
Disease	Mitochondrial encephalomyopathy
Variation	info
Gene
CLNDBN	Mitochondrial encephalomyopathy
Reversed	0
HGVS	NC_012920.1:m.3252A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010217.2,