rs863224181

Orientation

minus

Stabilized

minus

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

Make rs863224181(A;A)

Make rs863224181(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

87514493

Gene

RARS2

is a	snp
is	mentioned by
dbSNP	rs863224181
dbSNP (classic)	rs863224181
ClinGen	rs863224181
ebi	rs863224181
HLI	rs863224181
Exac	rs863224181
Gnomad	rs863224181
Varsome	rs863224181
LitVar	rs863224181
Map	rs863224181
PheGenI	rs863224181
Biobank	rs863224181
1000 genomes	rs863224181
hgdp	rs863224181
ensembl	rs863224181
geneview	rs863224181
scholar	rs863224181
google	rs863224181
pharmgkb	rs863224181
gwascentral	rs863224181
openSNP	rs863224181
23andMe	rs863224181
SNPshot	rs863224181
SNPdbe	rs863224181
MSV3d	rs863224181
GWAS Ctlg	rs863224181

Max Magnitude

0

ClinVar
Risk	rs863224181(A;A)
Alt	rs863224181(A;A)
Reference	Rs863224181(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RARS2
CLNDBN	not provided
Reversed	1
HGVS	NC_000006.11:g.88224211G>T
CLNSRC
CLNACC	RCV000195917.1,