rs1060499741

Orientation

plus

Stabilized

plus

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

Make rs1060499741(-;-)

Make rs1060499741(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

117255281

Gene

SLC18A2

is a	snp
is	mentioned by
dbSNP	rs1060499741
dbSNP (classic)	rs1060499741
ClinGen	rs1060499741
ebi	rs1060499741
HLI	rs1060499741
Exac	rs1060499741
Gnomad	rs1060499741
Varsome	rs1060499741
LitVar	rs1060499741
Map	rs1060499741
PheGenI	rs1060499741
Biobank	rs1060499741
1000 genomes	rs1060499741
hgdp	rs1060499741
ensembl	rs1060499741
geneview	rs1060499741
scholar	rs1060499741
google	rs1060499741
pharmgkb	rs1060499741
gwascentral	rs1060499741
openSNP	rs1060499741
23andMe	rs1060499741
SNPshot	rs1060499741
SNPdbe	rs1060499741
MSV3d	rs1060499741
GWAS Ctlg	rs1060499741

Max Magnitude

0

ClinVar
Risk	rs1060499741(-;-)
Alt	rs1060499741(-;-)
Reference	Rs1060499741(C;C)
Significance	Probable-Pathogenic
Disease	Abnormality of brain morphology
Variation	info
Gene	SLC18A2
CLNDBN	Abnormality of brain morphology
Reversed	0
HGVS	NC_000010.10:g.119014792delC
CLNSRC
CLNACC	RCV000454269.1,