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

rs483352689

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs483352689(G;G)
Make rs483352689(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48459721
GeneRB1
is asnp
is mentioned by
dbSNPrs483352689
ebirs483352689
HLIrs483352689
Exacrs483352689
Varsomers483352689
Maprs483352689
PheGenIrs483352689
hapmaprs483352689
1000 genomesrs483352689
hgdprs483352689
ensemblrs483352689
gopubmedrs483352689
geneviewrs483352689
scholarrs483352689
googlers483352689
pharmgkbrs483352689
gwascentralrs483352689
openSNPrs483352689
23andMers483352689
23andMe allrs483352689
SNP Nexus

SNPshotrs483352689
SNPdbers483352689
MSV3drs483352689
GWAS Ctlgrs483352689
Max Magnitude0
ClinVar
Risk rs483352689(G;G)
Alt rs483352689(G;G)
Reference rs483352689(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RB1
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.49033857T>G
CLNSRC
CLNACC RCV000087167.2,