rs879253874

Orientation

plus

Stabilized

plus

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

Make rs879253874(G;T)

Make rs879253874(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

12

Position

32731492

Gene	DNM1L, YARS2

is a	snp
is	mentioned by
dbSNP	rs879253874
dbSNP (classic)	rs879253874
ClinGen	rs879253874
ebi	rs879253874
HLI	rs879253874
Exac	rs879253874
Gnomad	rs879253874
Varsome	rs879253874
LitVar	rs879253874
Map	rs879253874
PheGenI	rs879253874
Biobank	rs879253874
1000 genomes	rs879253874
hgdp	rs879253874
ensembl	rs879253874
geneview	rs879253874
scholar	rs879253874
google	rs879253874
pharmgkb	rs879253874
gwascentral	rs879253874
openSNP	rs879253874
23andMe	rs879253874
SNPshot	rs879253874
SNPdbe	rs879253874
MSV3d	rs879253874
GWAS Ctlg	rs879253874

Max Magnitude

0

ClinVar
Risk	rs879253874(T;T)
Alt	rs879253874(T;T)
Reference	Rs879253874(G;G)
Significance	Probable-Pathogenic
Disease	Encephalopathy due to defective mitochondrial and peroxisomal fission 1
Variation	info
Gene	YARS2 DNM1L
CLNDBN	Encephalopathy due to defective mitochondrial and peroxisomal fission 1
Reversed	0
HGVS	NC_000012.11:g.32884426G>T
CLNSRC
CLNACC	RCV000237095.1,