rs863224040

Orientation

plus

Stabilized

plus

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

Make rs863224040(A;A)

Make rs863224040(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

140695846

Gene

HARS2

is a	snp
is	mentioned by
dbSNP	rs863224040
dbSNP (classic)	rs863224040
ClinGen	rs863224040
ebi	rs863224040
HLI	rs863224040
Exac	rs863224040
Gnomad	rs863224040
Varsome	rs863224040
LitVar	rs863224040
Map	rs863224040
PheGenI	rs863224040
Biobank	rs863224040
1000 genomes	rs863224040
hgdp	rs863224040
ensembl	rs863224040
geneview	rs863224040
scholar	rs863224040
google	rs863224040
pharmgkb	rs863224040
gwascentral	rs863224040
openSNP	rs863224040
23andMe	rs863224040
SNPshot	rs863224040
SNPdbe	rs863224040
MSV3d	rs863224040
GWAS Ctlg	rs863224040

Max Magnitude

0

ClinVar
Risk	rs863224040(A;A)
Alt	rs863224040(A;A)
Reference	Rs863224040(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	HARS2
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.140075431G>A
CLNSRC
CLNACC	RCV000195718.1,