rs863224182

Orientation

minus

Stabilized

minus

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

Make rs863224182(-;G)

Make rs863224182(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

87524632

Gene

RARS2

is a	snp
is	mentioned by
dbSNP	rs863224182
dbSNP (classic)	rs863224182
ClinGen	rs863224182
ebi	rs863224182
HLI	rs863224182
Exac	rs863224182
Gnomad	rs863224182
Varsome	rs863224182
LitVar	rs863224182
Map	rs863224182
PheGenI	rs863224182
Biobank	rs863224182
1000 genomes	rs863224182
hgdp	rs863224182
ensembl	rs863224182
geneview	rs863224182
scholar	rs863224182
google	rs863224182
pharmgkb	rs863224182
gwascentral	rs863224182
openSNP	rs863224182
23andMe	rs863224182
SNPshot	rs863224182
SNPdbe	rs863224182
MSV3d	rs863224182
GWAS Ctlg	rs863224182

Max Magnitude

0

ClinVar
Risk	rs863224182(G;G)
Alt	rs863224182(G;G)
Reference	Rs863224182(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	RARS2
CLNDBN	not provided
Reversed	1
HGVS	NC_000006.11:g.88234351dupC
CLNSRC
CLNACC	RCV000199506.1,