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rs587777158

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777158(A;A)
Make rs587777158(A;G)
ReferenceGRCh38 38.1/142
Chromosome20
Position445095
GeneTBC1D20
is asnp
is mentioned by
dbSNPrs587777158
ebirs587777158
HLIrs587777158
Exacrs587777158
Varsomers587777158
Maprs587777158
PheGenIrs587777158
hapmaprs587777158
1000 genomesrs587777158
hgdprs587777158
ensemblrs587777158
gopubmedrs587777158
geneviewrs587777158
scholarrs587777158
googlers587777158
pharmgkbrs587777158
gwascentralrs587777158
openSNPrs587777158
23andMers587777158
23andMe allrs587777158
SNP Nexus

SNPshotrs587777158
SNPdbers587777158
MSV3drs587777158
GWAS Ctlgrs587777158
Max Magnitude0
ClinVar
Risk rs587777158(A,G;A,G)
Alt rs587777158(A,G;A,G)
Reference rs587777158(C;C)
Significance Pathogenic
Disease Warburg micro syndrome 4
Variation info
Gene TBC1D20
CLNDBN Warburg micro syndrome 4
Reversed 1
HGVS NC_000020.10:g.425739G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000087139.3,