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

rs200910834

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200910834(C;C)
Make rs200910834(C;G)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position99727157
GeneCOX15
is asnp
is mentioned by
dbSNPrs200910834
dbSNP (old)rs200910834
ClinGenrs200910834
ebirs200910834
HLIrs200910834
Exacrs200910834
Gnomadrs200910834
Varsomers200910834
LitVarrs200910834
Maprs200910834
PheGenIrs200910834
Biobankrs200910834
1000 genomesrs200910834
hgdprs200910834
ensemblrs200910834
gopubmedrs200910834
geneviewrs200910834
scholarrs200910834
googlers200910834
pharmgkbrs200910834
gwascentralrs200910834
openSNPrs200910834
23andMers200910834
23andMe allrs200910834
SNPshotrs200910834
SNPdbers200910834
MSV3drs200910834
GWAS Ctlgrs200910834
Max Magnitude0
ClinVar
Risk rs200910834(C;C)
Alt rs200910834(C;C)
Reference Rs200910834(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COX15
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.101486914G>C
CLNSRC
CLNACC RCV000266470.1,