rs1060499743

Orientation

minus

Stabilized

minus

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

Make rs1060499743(G;G)

Make rs1060499743(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

24596030

Gene

ARHGAP21

is a	snp
is	mentioned by
dbSNP	rs1060499743
dbSNP (classic)	rs1060499743
ClinGen	rs1060499743
ebi	rs1060499743
HLI	rs1060499743
Exac	rs1060499743
Gnomad	rs1060499743
Varsome	rs1060499743
LitVar	rs1060499743
Map	rs1060499743
PheGenI	rs1060499743
Biobank	rs1060499743
1000 genomes	rs1060499743
hgdp	rs1060499743
ensembl	rs1060499743
geneview	rs1060499743
scholar	rs1060499743
google	rs1060499743
pharmgkb	rs1060499743
gwascentral	rs1060499743
openSNP	rs1060499743
23andMe	rs1060499743
SNPshot	rs1060499743
SNPdbe	rs1060499743
MSV3d	rs1060499743
GWAS Ctlg	rs1060499743

Max Magnitude

0

ClinVar
Risk	rs1060499743(G;G)
Alt	rs1060499743(G;G)
Reference	Rs1060499743(T;T)
Significance	Probable-Pathogenic
Disease	Abnormality of brain morphology
Variation	info
Gene	ARHGAP21
CLNDBN	Abnormality of brain morphology
Reversed	1
HGVS	NC_000010.10:g.24884959A>C
CLNSRC
CLNACC	RCV000454179.1,