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rs587777152

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777152(A;A)
Make rs587777152(A;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position135126250
GeneRAB3GAP1
is asnp
is mentioned by
dbSNPrs587777152
ebirs587777152
HLIrs587777152
Exacrs587777152
Varsomers587777152
Maprs587777152
PheGenIrs587777152
hapmaprs587777152
1000 genomesrs587777152
hgdprs587777152
ensemblrs587777152
gopubmedrs587777152
geneviewrs587777152
scholarrs587777152
googlers587777152
pharmgkbrs587777152
gwascentralrs587777152
openSNPrs587777152
23andMers587777152
23andMe allrs587777152
SNP Nexus

SNPshotrs587777152
SNPdbers587777152
MSV3drs587777152
GWAS Ctlgrs587777152
Max Magnitude0
ClinVar
Risk rs587777152(A;A)
Alt rs587777152(A;A)
Reference rs587777152(G;G)
Significance Pathogenic
Disease Warburg micro syndrome 1
Variation info
Gene RAB3GAP1
CLNDBN Warburg micro syndrome 1
Reversed 0
HGVS NC_000002.11:g.135883820G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000087133.4,