rs201392711

Orientation

plus

Stabilized

plus

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

Make rs201392711(A;G)

Make rs201392711(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

140693654

Gene	HARS, HARS2

is a	snp
is	mentioned by
dbSNP	rs201392711
dbSNP (classic)	rs201392711
ClinGen	rs201392711
ebi	rs201392711
HLI	rs201392711
Exac	rs201392711
Gnomad	rs201392711
Varsome	rs201392711
LitVar	rs201392711
Map	rs201392711
PheGenI	rs201392711
Biobank	rs201392711
1000 genomes	rs201392711
hgdp	rs201392711
ensembl	rs201392711
geneview	rs201392711
scholar	rs201392711
google	rs201392711
pharmgkb	rs201392711
gwascentral	rs201392711
openSNP	rs201392711
23andMe	rs201392711
SNPshot	rs201392711
SNPdbe	rs201392711
MSV3d	rs201392711
GWAS Ctlg	rs201392711

Max Magnitude

0

ClinVar
Risk	rs201392711(G;G)
Alt	rs201392711(G;G)
Reference	Rs201392711(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HARS HARS2
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.140073239A>G
CLNSRC
CLNACC	RCV000197397.1,