rs1057522050

Orientation

minus

Stabilized

minus

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

Make rs1057522050(C;C)

Make rs1057522050(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

87514991

Gene

RARS2

is a	snp
is	mentioned by
dbSNP	rs1057522050
dbSNP (classic)	rs1057522050
ClinGen	rs1057522050
ebi	rs1057522050
HLI	rs1057522050
Exac	rs1057522050
Gnomad	rs1057522050
Varsome	rs1057522050
LitVar	rs1057522050
Map	rs1057522050
PheGenI	rs1057522050
Biobank	rs1057522050
1000 genomes	rs1057522050
hgdp	rs1057522050
ensembl	rs1057522050
geneview	rs1057522050
scholar	rs1057522050
google	rs1057522050
pharmgkb	rs1057522050
gwascentral	rs1057522050
openSNP	rs1057522050
23andMe	rs1057522050
SNPshot	rs1057522050
SNPdbe	rs1057522050
MSV3d	rs1057522050
GWAS Ctlg	rs1057522050

Max Magnitude

0

ClinVar
Risk	rs1057522050(C;C)
Alt	rs1057522050(C;C)
Reference	Rs1057522050(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RARS2
CLNDBN	not provided
Reversed	1
HGVS	NC_000006.11:g.88224709A>G
CLNSRC
CLNACC	RCV000417917.1,