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

rs786205528

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205528(C;T)
Make rs786205528(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position96115486
GeneADRA2B
is asnp
is mentioned by
dbSNPrs786205528
ebirs786205528
HLIrs786205528
Exacrs786205528
Varsomers786205528
Maprs786205528
PheGenIrs786205528
hapmaprs786205528
1000 genomesrs786205528
hgdprs786205528
ensemblrs786205528
gopubmedrs786205528
geneviewrs786205528
scholarrs786205528
googlers786205528
pharmgkbrs786205528
gwascentralrs786205528
openSNPrs786205528
23andMers786205528
23andMe allrs786205528
SNP Nexus

SNPshotrs786205528
SNPdbers786205528
MSV3drs786205528
GWAS Ctlgrs786205528
Max Magnitude0
ClinVar
Risk rs786205528(T;T)
Alt rs786205528(T;T)
Reference rs786205528(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ADRA2B
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.96781225G>A
CLNSRC
CLNACC RCV000171297.1,