rs1060499736

Orientation

minus

Stabilized

minus

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

Make rs1060499736(C;T)

Make rs1060499736(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

129523364

Gene

SMARCA1

is a	snp
is	mentioned by
dbSNP	rs1060499736
dbSNP (classic)	rs1060499736
ClinGen	rs1060499736
ebi	rs1060499736
HLI	rs1060499736
Exac	rs1060499736
Gnomad	rs1060499736
Varsome	rs1060499736
LitVar	rs1060499736
Map	rs1060499736
PheGenI	rs1060499736
Biobank	rs1060499736
1000 genomes	rs1060499736
hgdp	rs1060499736
ensembl	rs1060499736
geneview	rs1060499736
scholar	rs1060499736
google	rs1060499736
pharmgkb	rs1060499736
gwascentral	rs1060499736
openSNP	rs1060499736
23andMe	rs1060499736
SNPshot	rs1060499736
SNPdbe	rs1060499736
MSV3d	rs1060499736
GWAS Ctlg	rs1060499736

Max Magnitude

0

ClinVar
Risk	rs1060499736(T;T)
Alt	rs1060499736(T;T)
Reference	Rs1060499736(C;C)
Significance	Probable-Pathogenic
Disease	Abnormality of brain morphology
Variation	info
Gene	SMARCA1
CLNDBN	Abnormality of brain morphology
Reversed	1
HGVS	NC_000023.10:g.128657341G>A
CLNSRC
CLNACC	RCV000454288.1,