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rs766629205

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766629205(C;T)
Make rs766629205(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position135130030
GeneRAB3GAP1
is asnp
is mentioned by
dbSNPrs766629205
ebirs766629205
HLIrs766629205
Exacrs766629205
Varsomers766629205
Maprs766629205
PheGenIrs766629205
hapmaprs766629205
1000 genomesrs766629205
hgdprs766629205
ensemblrs766629205
gopubmedrs766629205
geneviewrs766629205
scholarrs766629205
googlers766629205
pharmgkbrs766629205
gwascentralrs766629205
openSNPrs766629205
23andMers766629205
23andMe allrs766629205
SNP Nexus

SNPshotrs766629205
SNPdbers766629205
MSV3drs766629205
GWAS Ctlgrs766629205
Max Magnitude0
ClinVar
Risk rs766629205(T;T)
Alt rs766629205(T;T)
Reference rs766629205(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAB3GAP1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.135887600C>T
CLNSRC
CLNACC RCV000171306.1,