rs765044856

Orientation

plus

Stabilized

plus

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

Make rs765044856(C;T)

Make rs765044856(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

87524578

Gene

RARS2

is a	snp
is	mentioned by
dbSNP	rs765044856
dbSNP (classic)	rs765044856
ClinGen	rs765044856
ebi	rs765044856
HLI	rs765044856
Exac	rs765044856
Gnomad	rs765044856
Varsome	rs765044856
LitVar	rs765044856
Map	rs765044856
PheGenI	rs765044856
Biobank	rs765044856
1000 genomes	rs765044856
hgdp	rs765044856
ensembl	rs765044856
geneview	rs765044856
scholar	rs765044856
google	rs765044856
pharmgkb	rs765044856
gwascentral	rs765044856
openSNP	rs765044856
23andMe	rs765044856
SNPshot	rs765044856
SNPdbe	rs765044856
MSV3d	rs765044856
GWAS Ctlg	rs765044856

Max Magnitude

0

ClinVar
Risk	rs765044856(T;T)
Alt	rs765044856(T;T)
Reference	Rs765044856(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RARS2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.88234296C>T
CLNSRC
CLNACC	RCV000197178.1,