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rs786205902

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205902(A;A)
Make rs786205902(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position180803571
GeneXPR1
is asnp
is mentioned by
dbSNPrs786205902
ebirs786205902
HLIrs786205902
Exacrs786205902
Varsomers786205902
Maprs786205902
PheGenIrs786205902
hapmaprs786205902
1000 genomesrs786205902
hgdprs786205902
ensemblrs786205902
gopubmedrs786205902
geneviewrs786205902
scholarrs786205902
googlers786205902
pharmgkbrs786205902
gwascentralrs786205902
openSNPrs786205902
23andMers786205902
23andMe allrs786205902
SNP Nexus

SNPshotrs786205902
SNPdbers786205902
MSV3drs786205902
GWAS Ctlgrs786205902
Max Magnitude0
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
CLNACC RCV000172880.2,