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rs786205492

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205492(A;A)
Make rs786205492(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position43056367
GeneUBR1
is asnp
is mentioned by
dbSNPrs786205492
ebirs786205492
HLIrs786205492
Exacrs786205492
Varsomers786205492
Maprs786205492
PheGenIrs786205492
hapmaprs786205492
1000 genomesrs786205492
hgdprs786205492
ensemblrs786205492
gopubmedrs786205492
geneviewrs786205492
scholarrs786205492
googlers786205492
pharmgkbrs786205492
gwascentralrs786205492
openSNPrs786205492
23andMers786205492
23andMe allrs786205492
SNP Nexus

SNPshotrs786205492
SNPdbers786205492
MSV3drs786205492
GWAS Ctlgrs786205492
Max Magnitude0
ClinVar
Risk rs786205492(A;A)
Alt rs786205492(A;A)
Reference rs786205492(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene UBR1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.43348565G>T
CLNSRC
CLNACC RCV000171234.1,