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rs1064795547

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Chromosome6
Position149378828
GeneTAB2
is asnp
is mentioned by
dbSNPrs1064795547
dbSNP (classic)rs1064795547
ClinGenrs1064795547
ebirs1064795547
HLIrs1064795547
Exacrs1064795547
Gnomadrs1064795547
Varsomers1064795547
LitVarrs1064795547
Maprs1064795547
PheGenIrs1064795547
Biobankrs1064795547
1000 genomesrs1064795547
hgdprs1064795547
ensemblrs1064795547
geneviewrs1064795547
scholarrs1064795547
googlers1064795547
pharmgkbrs1064795547
gwascentralrs1064795547
openSNPrs1064795547
23andMers1064795547
23andMe allrs1064795547
SNPshotrs1064795547
SNPdbers1064795547
MSV3drs1064795547
GWAS Ctlgrs1064795547
Max Magnitude0
ClinVar
Risk rs1064795547(-;-)
Alt rs1064795547(-;-)
Reference Rs1064795547(CA;CA)
Significance Pathogenic
Disease not provided
Variation info
Gene TAB2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.149699964_149699965delCA
CLNSRC
CLNACC RCV000487063.1,