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

rs864309615

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309615(A;A)
Make rs864309615(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position157181168
GeneARID1B
is asnp
is mentioned by
dbSNPrs864309615
ebirs864309615
HLIrs864309615
Exacrs864309615
Varsomers864309615
Maprs864309615
PheGenIrs864309615
hapmaprs864309615
1000 genomesrs864309615
hgdprs864309615
ensemblrs864309615
gopubmedrs864309615
geneviewrs864309615
scholarrs864309615
googlers864309615
pharmgkbrs864309615
gwascentralrs864309615
openSNPrs864309615
23andMers864309615
23andMe allrs864309615
SNP Nexus

SNPshotrs864309615
SNPdbers864309615
MSV3drs864309615
GWAS Ctlgrs864309615
Max Magnitude0
ClinVar
Risk rs864309615(A;A)
Alt rs864309615(A;A)
Reference rs864309615(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ARID1B
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.157502302G>A
CLNSRC
CLNACC RCV000202727.1,