rs1060499751

Orientation

plus

Stabilized

plus

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

Make rs1060499751(C;T)

Make rs1060499751(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

153659157

Gene

SNAPIN

is a	snp
is	mentioned by
dbSNP	rs1060499751
dbSNP (classic)	rs1060499751
ClinGen	rs1060499751
ebi	rs1060499751
HLI	rs1060499751
Exac	rs1060499751
Gnomad	rs1060499751
Varsome	rs1060499751
LitVar	rs1060499751
Map	rs1060499751
PheGenI	rs1060499751
Biobank	rs1060499751
1000 genomes	rs1060499751
hgdp	rs1060499751
ensembl	rs1060499751
geneview	rs1060499751
scholar	rs1060499751
google	rs1060499751
pharmgkb	rs1060499751
gwascentral	rs1060499751
openSNP	rs1060499751
23andMe	rs1060499751
SNPshot	rs1060499751
SNPdbe	rs1060499751
MSV3d	rs1060499751
GWAS Ctlg	rs1060499751

Max Magnitude

0

ClinVar
Risk	rs1060499751(T;T)
Alt	rs1060499751(T;T)
Reference	Rs1060499751(C;C)
Significance	Probable-Pathogenic
Disease	Abnormality of brain morphology
Variation	info
Gene	SNAPIN
CLNDBN	Abnormality of brain morphology
Reversed	0
HGVS	NC_000001.10:g.153631633C>T
CLNSRC
CLNACC	RCV000454257.1,