rs587777215

Orientation

plus

Stabilized

minus

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

Make rs587777215(C;C)

Make rs587777215(C;T)

Reference

GRCh38 38.1/142

Chromosome

12

Position

32747335

Gene

YARS2

is a	snp
is	mentioned by
dbSNP	rs587777215
dbSNP (classic)	rs587777215
ClinGen	rs587777215
ebi	rs587777215
HLI	rs587777215
Exac	rs587777215
Gnomad	rs587777215
Varsome	rs587777215
LitVar	rs587777215
Map	rs587777215
PheGenI	rs587777215
Biobank	rs587777215
1000 genomes	rs587777215
hgdp	rs587777215
ensembl	rs587777215
geneview	rs587777215
scholar	rs587777215
google	rs587777215
pharmgkb	rs587777215
gwascentral	rs587777215
openSNP	rs587777215
23andMe	rs587777215
SNPshot	rs587777215
SNPdbe	rs587777215
MSV3d	rs587777215
GWAS Ctlg	rs587777215

Max Magnitude

0

ClinVar
Risk	rs587777215(C;C) Rs587777215(T;T)
Alt	rs587777215(C;C) Rs587777215(T;T)
Reference	Rs587777215(A;A)
Significance	Pathogenic
Disease	Myopathy
Variation	info
Gene	YARS2
CLNDBN	Myopathy, lactic acidosis, and sideroblastic anemia 2
Reversed	1
HGVS	NC_000012.11:g.32900269T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000088674.3,