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rs886041646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome6
Position149379301
GeneTAB2
is asnp
is mentioned by
dbSNPrs886041646
dbSNP (classic)rs886041646
ClinGenrs886041646
ebirs886041646
HLIrs886041646
Exacrs886041646
Gnomadrs886041646
Varsomers886041646
LitVarrs886041646
Maprs886041646
PheGenIrs886041646
Biobankrs886041646
1000 genomesrs886041646
hgdprs886041646
ensemblrs886041646
geneviewrs886041646
scholarrs886041646
googlers886041646
pharmgkbrs886041646
gwascentralrs886041646
openSNPrs886041646
23andMers886041646
SNPshotrs886041646
SNPdbers886041646
MSV3drs886041646
GWAS Ctlgrs886041646
Max Magnitude0
ClinVar
Risk rs886041646(-;-)
Alt rs886041646(-;-)
Reference Rs886041646(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TAB2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.149700437delC
CLNSRC
CLNACC RCV000266578.1,