rs145297855

Orientation

plus

Stabilized

plus

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

Make rs145297855(C;T)

Make rs145297855(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

87529647

Gene

RARS2

is a	snp
is	mentioned by
dbSNP	rs145297855
dbSNP (classic)	rs145297855
ClinGen	rs145297855
ebi	rs145297855
HLI	rs145297855
Exac	rs145297855
Gnomad	rs145297855
Varsome	rs145297855
LitVar	rs145297855
Map	rs145297855
PheGenI	rs145297855
Biobank	rs145297855
1000 genomes	rs145297855
hgdp	rs145297855
ensembl	rs145297855
geneview	rs145297855
scholar	rs145297855
google	rs145297855
pharmgkb	rs145297855
gwascentral	rs145297855
openSNP	rs145297855
23andMe	rs145297855
SNPshot	rs145297855
SNPdbe	rs145297855
MSV3d	rs145297855
GWAS Ctlg	rs145297855

Max Magnitude

0

ClinVar
Risk	rs145297855(A;A) rs145297855(T;T)
Alt	rs145297855(A;A) rs145297855(T;T)
Reference	Rs145297855(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	RARS2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.88239365C>T
CLNSRC
CLNACC	RCV000198712.1,