rs786205902

Orientation

plus

Stabilized

plus

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

Make rs786205902(A;A)

Make rs786205902(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

180803571

Gene

XPR1

is a	snp
is	mentioned by
dbSNP	rs786205902
dbSNP (classic)	rs786205902
ClinGen	rs786205902
ebi	rs786205902
HLI	rs786205902
Exac	rs786205902
Gnomad	rs786205902
Varsome	rs786205902
LitVar	rs786205902
Map	rs786205902
PheGenI	rs786205902
Biobank	rs786205902
1000 genomes	rs786205902
hgdp	rs786205902
ensembl	rs786205902
geneview	rs786205902
scholar	rs786205902
google	rs786205902
pharmgkb	rs786205902
gwascentral	rs786205902
openSNP	rs786205902
23andMe	rs786205902
SNPshot	rs786205902
SNPdbe	rs786205902
MSV3d	rs786205902
GWAS Ctlg	rs786205902

Max Magnitude

0

ClinVar
Risk	rs786205902(A;A)
Alt	rs786205902(A;A)
Reference	Rs786205902(G;G)
Significance	Pathogenic
Disease	Basal ganglia calcification
Variation	info
Gene	XPR1
CLNDBN	Basal ganglia calcification, idiopathic, 6
Reversed	0
HGVS	NC_000001.10:g.180772707G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000172880.2,