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

rs587777169

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777169(A;A)
Make rs587777169(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position220153976
GeneRAB3GAP2
is asnp
is mentioned by
dbSNPrs587777169
ebirs587777169
HLIrs587777169
Exacrs587777169
Varsomers587777169
Maprs587777169
PheGenIrs587777169
hapmaprs587777169
1000 genomesrs587777169
hgdprs587777169
ensemblrs587777169
gopubmedrs587777169
geneviewrs587777169
scholarrs587777169
googlers587777169
pharmgkbrs587777169
gwascentralrs587777169
openSNPrs587777169
23andMers587777169
23andMe allrs587777169
SNP Nexus

SNPshotrs587777169
SNPdbers587777169
MSV3drs587777169
GWAS Ctlgrs587777169
Max Magnitude0
ClinVar
Risk rs587777169(A;A)
Alt rs587777169(A;A)
Reference rs587777169(G;G)
Significance Pathogenic
Disease Warburg micro syndrome 2
Variation info
Gene RAB3GAP2
CLNDBN Warburg micro syndrome 2
Reversed 0
HGVS NC_000001.10:g.220327318G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000087152.3,