rs863223957

Orientation

plus

Stabilized

plus

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

Make rs863223957(A;A)

Make rs863223957(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

5545264

Gene

FARS2

is a	snp
is	mentioned by
dbSNP	rs863223957
dbSNP (classic)	rs863223957
ClinGen	rs863223957
ebi	rs863223957
HLI	rs863223957
Exac	rs863223957
Gnomad	rs863223957
Varsome	rs863223957
LitVar	rs863223957
Map	rs863223957
PheGenI	rs863223957
Biobank	rs863223957
1000 genomes	rs863223957
hgdp	rs863223957
ensembl	rs863223957
geneview	rs863223957
scholar	rs863223957
google	rs863223957
pharmgkb	rs863223957
gwascentral	rs863223957
openSNP	rs863223957
23andMe	rs863223957
SNPshot	rs863223957
SNPdbe	rs863223957
MSV3d	rs863223957
GWAS Ctlg	rs863223957

Max Magnitude

0

ClinVar
Risk	rs863223957(A;A) rs863223957(C;C)
Alt	rs863223957(A;A) rs863223957(C;C)
Reference	Rs863223957(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	FARS2
CLNDBN	not specified
Reversed	0
HGVS	NC_000006.11:g.5545497G>A
CLNSRC
CLNACC	RCV000198248.1,