Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064795718

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome18
Position23560391
GeneNPC1
is asnp
is mentioned by
dbSNPrs1064795718
dbSNP (classic)rs1064795718
ClinGenrs1064795718
ebirs1064795718
HLIrs1064795718
Exacrs1064795718
Gnomadrs1064795718
Varsomers1064795718
LitVarrs1064795718
Maprs1064795718
PheGenIrs1064795718
Biobankrs1064795718
1000 genomesrs1064795718
hgdprs1064795718
ensemblrs1064795718
geneviewrs1064795718
scholarrs1064795718
googlers1064795718
pharmgkbrs1064795718
gwascentralrs1064795718
openSNPrs1064795718
23andMers1064795718
SNPshotrs1064795718
SNPdbers1064795718
MSV3drs1064795718
GWAS Ctlgrs1064795718
Max Magnitude0
ClinVar
Risk rs1064795718(T;T)
Alt rs1064795718(T;T)
Reference Rs1064795718(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NPC1
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.21140355G>A
CLNSRC
CLNACC RCV000478255.1,