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rs137853053

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853053(A;A)
Make rs137853053(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position135135743
GeneRAB3GAP1
is asnp
is mentioned by
dbSNPrs137853053
ebirs137853053
HLIrs137853053
Exacrs137853053
Varsomers137853053
Maprs137853053
PheGenIrs137853053
hapmaprs137853053
1000 genomesrs137853053
hgdprs137853053
ensemblrs137853053
gopubmedrs137853053
geneviewrs137853053
scholarrs137853053
googlers137853053
pharmgkbrs137853053
gwascentralrs137853053
openSNPrs137853053
23andMers137853053
23andMe allrs137853053
SNP Nexus

SNPshotrs137853053
SNPdbers137853053
MSV3drs137853053
GWAS Ctlgrs137853053
Max Magnitude0
OMIM602536
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137853053(A;A)
Alt rs137853053(A;A)
Reference rs137853053(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.135893313G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007476.3,