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rs869312704

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869312704(-;-)
Make rs869312704(-;GGCTGCA)
Make rs869312704(GGCTGCA;GGCTGCA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position161423772
GeneTBR1
is asnp
is mentioned by
dbSNPrs869312704
ebirs869312704
HLIrs869312704
Exacrs869312704
Varsomers869312704
Maprs869312704
PheGenIrs869312704
hapmaprs869312704
1000 genomesrs869312704
hgdprs869312704
ensemblrs869312704
gopubmedrs869312704
geneviewrs869312704
scholarrs869312704
googlers869312704
pharmgkbrs869312704
gwascentralrs869312704
openSNPrs869312704
23andMers869312704
23andMe allrs869312704
SNP Nexus

SNPshotrs869312704
SNPdbers869312704
MSV3drs869312704
GWAS Ctlgrs869312704
Max Magnitude0
ClinVar
Risk rs869312704(GCTGCAG;GCTGCAG)
Alt rs869312704(GCTGCAG;GCTGCAG)
Reference rs869312704(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TBR1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.162280277_162280283dupGGCTGCA
CLNSRC
CLNACC RCV000209932.1,