rs201650281

Orientation

plus

Stabilized

plus

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

Make rs201650281(A;A)

Make rs201650281(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

75635982

Gene

KARS

is a	snp
is	mentioned by
dbSNP	rs201650281
dbSNP (classic)	rs201650281
ClinGen	rs201650281
ebi	rs201650281
HLI	rs201650281
Exac	rs201650281
Gnomad	rs201650281
Varsome	rs201650281
LitVar	rs201650281
Map	rs201650281
PheGenI	rs201650281
Biobank	rs201650281
1000 genomes	rs201650281
hgdp	rs201650281
ensembl	rs201650281
geneview	rs201650281
scholar	rs201650281
google	rs201650281
pharmgkb	rs201650281
gwascentral	rs201650281
openSNP	rs201650281
23andMe	rs201650281
SNPshot	rs201650281
SNPdbe	rs201650281
MSV3d	rs201650281
GWAS Ctlg	rs201650281

Max Magnitude

0

ClinVar
Risk	rs201650281(A;A)
Alt	rs201650281(A;A)
Reference	Rs201650281(G;G)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	KARS
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000016.9:g.75669880G>A
CLNSRC
CLNACC	RCV000210691.1,