rs1060499772

Orientation

minus

Stabilized

minus

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

Make rs1060499772(C;C)

Make rs1060499772(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

135943412

Gene

DARS

is a	snp
is	mentioned by
dbSNP	rs1060499772
dbSNP (classic)	rs1060499772
ClinGen	rs1060499772
ebi	rs1060499772
HLI	rs1060499772
Exac	rs1060499772
Gnomad	rs1060499772
Varsome	rs1060499772
LitVar	rs1060499772
Map	rs1060499772
PheGenI	rs1060499772
Biobank	rs1060499772
1000 genomes	rs1060499772
hgdp	rs1060499772
ensembl	rs1060499772
geneview	rs1060499772
scholar	rs1060499772
google	rs1060499772
pharmgkb	rs1060499772
gwascentral	rs1060499772
openSNP	rs1060499772
23andMe	rs1060499772
SNPshot	rs1060499772
SNPdbe	rs1060499772
MSV3d	rs1060499772
GWAS Ctlg	rs1060499772

Max Magnitude

0

ClinVar
Risk	rs1060499772(C;C)
Alt	rs1060499772(C;C)
Reference	Rs1060499772(G;G)
Significance	Probable-Pathogenic
Disease	Abnormality of brain morphology
Variation	info
Gene	DARS
CLNDBN	Abnormality of brain morphology
Reversed	1
HGVS	NC_000002.11:g.136700982C>G
CLNSRC
CLNACC	RCV000454195.1,