rs374957295

Orientation

plus

Stabilized

plus

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

Make rs374957295(C;T)

Make rs374957295(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

5368893

Gene

FARS2

is a	snp
is	mentioned by
dbSNP	rs374957295
dbSNP (classic)	rs374957295
ClinGen	rs374957295
ebi	rs374957295
HLI	rs374957295
Exac	rs374957295
Gnomad	rs374957295
Varsome	rs374957295
LitVar	rs374957295
Map	rs374957295
PheGenI	rs374957295
Biobank	rs374957295
1000 genomes	rs374957295
hgdp	rs374957295
ensembl	rs374957295
geneview	rs374957295
scholar	rs374957295
google	rs374957295
pharmgkb	rs374957295
gwascentral	rs374957295
openSNP	rs374957295
23andMe	rs374957295
SNPshot	rs374957295
SNPdbe	rs374957295
MSV3d	rs374957295
GWAS Ctlg	rs374957295

Max Magnitude

0

ClinVar
Risk	rs374957295(G;G) rs374957295(T;T)
Alt	rs374957295(G;G) rs374957295(T;T)
Reference	Rs374957295(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FARS2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.5369126C>T
CLNSRC
CLNACC	RCV000199836.1,