rs786205901

Orientation

plus

Stabilized

plus

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

Make rs786205901(C;C)

Make rs786205901(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

180803598

Gene

XPR1

is a	snp
is	mentioned by
dbSNP	rs786205901
dbSNP (classic)	rs786205901
ClinGen	rs786205901
ebi	rs786205901
HLI	rs786205901
Exac	rs786205901
Gnomad	rs786205901
Varsome	rs786205901
LitVar	rs786205901
Map	rs786205901
PheGenI	rs786205901
Biobank	rs786205901
1000 genomes	rs786205901
hgdp	rs786205901
ensembl	rs786205901
geneview	rs786205901
scholar	rs786205901
google	rs786205901
pharmgkb	rs786205901
gwascentral	rs786205901
openSNP	rs786205901
23andMe	rs786205901
SNPshot	rs786205901
SNPdbe	rs786205901
MSV3d	rs786205901
GWAS Ctlg	rs786205901

Max Magnitude

0

ClinVar
Risk	rs786205901(C;C)
Alt	rs786205901(C;C)
Reference	Rs786205901(T;T)
Significance	Pathogenic
Disease	Basal ganglia calcification
Variation	info
Gene	XPR1
CLNDBN	Basal ganglia calcification, idiopathic, 6
Reversed	0
HGVS	NC_000001.10:g.180772734T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000172879.2,