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rs786205584

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205584(G;T)
Make rs786205584(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position157207091
GeneARID1B
is asnp
is mentioned by
dbSNPrs786205584
ebirs786205584
HLIrs786205584
Exacrs786205584
Varsomers786205584
Maprs786205584
PheGenIrs786205584
hapmaprs786205584
1000 genomesrs786205584
hgdprs786205584
ensemblrs786205584
gopubmedrs786205584
geneviewrs786205584
scholarrs786205584
googlers786205584
pharmgkbrs786205584
gwascentralrs786205584
openSNPrs786205584
23andMers786205584
23andMe allrs786205584
SNP Nexus

SNPshotrs786205584
SNPdbers786205584
MSV3drs786205584
GWAS Ctlgrs786205584
Max Magnitude0
ClinVar
Risk rs786205584(T;T)
Alt rs786205584(T;T)
Reference rs786205584(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ARID1B
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.157528225G>T
CLNSRC
CLNACC RCV000171404.1,