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rs727502810

From SNPedia

Orientationplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs727502810(-;-)
Make rs727502810(-;AG)
Make rs727502810(AG;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position8100580
GeneRIC3, TUB
is asnp
is mentioned by
dbSNPrs727502810
ebirs727502810
HLIrs727502810
Exacrs727502810
Varsomers727502810
Maprs727502810
PheGenIrs727502810
hapmaprs727502810
1000 genomesrs727502810
hgdprs727502810
ensemblrs727502810
gopubmedrs727502810
geneviewrs727502810
scholarrs727502810
googlers727502810
pharmgkbrs727502810
gwascentralrs727502810
openSNPrs727502810
23andMers727502810
23andMe allrs727502810
SNP Nexus

SNPshotrs727502810
SNPdbers727502810
MSV3drs727502810
GWAS Ctlgrs727502810
Max Magnitude0
ClinVar
Risk rs727502810(;)
Alt rs727502810(;)
Reference rs727502810(GA;GA)
Significance Pathogenic
Disease Retinal dystrophy and obesity
Variation info
Gene TUB
CLNDBN Retinal dystrophy and obesity
Reversed 0
HGVS NC_000011.9:g.8122127_8122128delAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000149873.4,