rs140540222

Orientation

plus

Stabilized

plus

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

Make rs140540222(C;T)

Make rs140540222(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

140695556

Gene

HARS2

is a	snp
is	mentioned by
dbSNP	rs140540222
dbSNP (classic)	rs140540222
ClinGen	rs140540222
ebi	rs140540222
HLI	rs140540222
Exac	rs140540222
Gnomad	rs140540222
Varsome	rs140540222
LitVar	rs140540222
Map	rs140540222
PheGenI	rs140540222
Biobank	rs140540222
1000 genomes	rs140540222
hgdp	rs140540222
ensembl	rs140540222
geneview	rs140540222
scholar	rs140540222
google	rs140540222
pharmgkb	rs140540222
gwascentral	rs140540222
openSNP	rs140540222
23andMe	rs140540222
SNPshot	rs140540222
SNPdbe	rs140540222
MSV3d	rs140540222
GWAS Ctlg	rs140540222

Max Magnitude

0

ClinVar
Risk	rs140540222(T;T)
Alt	rs140540222(T;T)
Reference	Rs140540222(C;C)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	HARS2
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000005.9:g.140075141C>T
CLNSRC
CLNACC	RCV000199285.1, RCV000223531.1,