rs797044855

Orientation

plus

Stabilized

plus

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

Make rs797044855(A;A)

Make rs797044855(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

30599995

Gene

GARS

is a	snp
is	mentioned by
dbSNP	rs797044855
dbSNP (classic)	rs797044855
ClinGen	rs797044855
ebi	rs797044855
HLI	rs797044855
Exac	rs797044855
Gnomad	rs797044855
Varsome	rs797044855
LitVar	rs797044855
Map	rs797044855
PheGenI	rs797044855
Biobank	rs797044855
1000 genomes	rs797044855
hgdp	rs797044855
ensembl	rs797044855
geneview	rs797044855
scholar	rs797044855
google	rs797044855
pharmgkb	rs797044855
gwascentral	rs797044855
openSNP	rs797044855
23andMe	rs797044855
SNPshot	rs797044855
SNPdbe	rs797044855
MSV3d	rs797044855
GWAS Ctlg	rs797044855

Max Magnitude

0

ClinVar
Risk	rs797044855(A;A)
Alt	rs797044855(A;A)
Reference	Rs797044855(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	GARS
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000007.13:g.30639611G>A
CLNSRC
CLNACC	RCV000190657.1,