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rs797045905

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045905(G;G)
Make rs797045905(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position135164629
GeneRAB3GAP1
is asnp
is mentioned by
dbSNPrs797045905
ebirs797045905
HLIrs797045905
Exacrs797045905
Varsomers797045905
Maprs797045905
PheGenIrs797045905
hapmaprs797045905
1000 genomesrs797045905
hgdprs797045905
ensemblrs797045905
gopubmedrs797045905
geneviewrs797045905
scholarrs797045905
googlers797045905
pharmgkbrs797045905
gwascentralrs797045905
openSNPrs797045905
23andMers797045905
23andMe allrs797045905
SNP Nexus

SNPshotrs797045905
SNPdbers797045905
MSV3drs797045905
GWAS Ctlgrs797045905
Max Magnitude0
ClinVar
Risk rs797045905(G;G)
Alt rs797045905(G;G)
Reference rs797045905(T;T)
Significance Pathogenic
Disease Warburg micro syndrome 1
Variation info
Gene RAB3GAP1
CLNDBN Warburg micro syndrome 1
Reversed 0
HGVS NC_000002.11:g.135922199T>G
CLNSRC
CLNACC RCV000194301.1,