rs757600616

Orientation

plus

Stabilized

plus

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

Make rs757600616(A;A)

Make rs757600616(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

119033279

Gene

WARS2

is a	snp
is	mentioned by
dbSNP	rs757600616
dbSNP (classic)	rs757600616
ClinGen	rs757600616
ebi	rs757600616
HLI	rs757600616
Exac	rs757600616
Gnomad	rs757600616
Varsome	rs757600616
LitVar	rs757600616
Map	rs757600616
PheGenI	rs757600616
Biobank	rs757600616
1000 genomes	rs757600616
hgdp	rs757600616
ensembl	rs757600616
geneview	rs757600616
scholar	rs757600616
google	rs757600616
pharmgkb	rs757600616
gwascentral	rs757600616
openSNP	rs757600616
23andMe	rs757600616
SNPshot	rs757600616
SNPdbe	rs757600616
MSV3d	rs757600616
GWAS Ctlg	rs757600616

Max Magnitude

0

ClinVar
Risk	rs757600616(A;A)
Alt	rs757600616(A;A)
Reference	Rs757600616(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	WARS2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.119575902G>A
CLNSRC
CLNACC	RCV000209871.1,