rs863223958

Orientation

plus

Stabilized

plus

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

Make rs863223958(C;G)

Make rs863223958(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

5368973

Gene

FARS2

is a	snp
is	mentioned by
dbSNP	rs863223958
dbSNP (classic)	rs863223958
ClinGen	rs863223958
ebi	rs863223958
HLI	rs863223958
Exac	rs863223958
Gnomad	rs863223958
Varsome	rs863223958
LitVar	rs863223958
Map	rs863223958
PheGenI	rs863223958
Biobank	rs863223958
1000 genomes	rs863223958
hgdp	rs863223958
ensembl	rs863223958
geneview	rs863223958
scholar	rs863223958
google	rs863223958
pharmgkb	rs863223958
gwascentral	rs863223958
openSNP	rs863223958
23andMe	rs863223958
SNPshot	rs863223958
SNPdbe	rs863223958
MSV3d	rs863223958
GWAS Ctlg	rs863223958

Max Magnitude

0

ClinVar
Risk	rs863223958(G;G)
Alt	rs863223958(G;G)
Reference	Rs863223958(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FARS2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.5369206C>G
CLNSRC
CLNACC	RCV000197422.1,