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rs187089611

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs187089611(C;C)
Make rs187089611(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position209877990
GeneUNC80
is asnp
is mentioned by
dbSNPrs187089611
ebirs187089611
HLIrs187089611
Exacrs187089611
Varsomers187089611
Maprs187089611
PheGenIrs187089611
hapmaprs187089611
1000 genomesrs187089611
hgdprs187089611
ensemblrs187089611
gopubmedrs187089611
geneviewrs187089611
scholarrs187089611
googlers187089611
pharmgkbrs187089611
gwascentralrs187089611
openSNPrs187089611
23andMers187089611
23andMe allrs187089611
SNP Nexus

SNPshotrs187089611
SNPdbers187089611
MSV3drs187089611
GWAS Ctlgrs187089611
Max Magnitude0
ClinVar
Risk rs187089611(C;C)
Alt rs187089611(C;C)
Reference rs187089611(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene UNC80
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000002.11:g.210742714G>C
CLNSRC
CLNACC RCV000210574.1,