rs372054960

Orientation

plus

Stabilized

plus

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

Make rs372054960(C;T)

Make rs372054960(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

5771293

Gene

FARS2

is a	snp
is	mentioned by
dbSNP	rs372054960
dbSNP (classic)	rs372054960
ClinGen	rs372054960
ebi	rs372054960
HLI	rs372054960
Exac	rs372054960
Gnomad	rs372054960
Varsome	rs372054960
LitVar	rs372054960
Map	rs372054960
PheGenI	rs372054960
Biobank	rs372054960
1000 genomes	rs372054960
hgdp	rs372054960
ensembl	rs372054960
geneview	rs372054960
scholar	rs372054960
google	rs372054960
pharmgkb	rs372054960
gwascentral	rs372054960
openSNP	rs372054960
23andMe	rs372054960
SNPshot	rs372054960
SNPdbe	rs372054960
MSV3d	rs372054960
GWAS Ctlg	rs372054960

Max Magnitude

0

ClinVar
Risk	rs372054960(T;T)
Alt	rs372054960(T;T)
Reference	Rs372054960(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FARS2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.5771526C>T
CLNSRC
CLNACC	RCV000198201.1,