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rs1064796285

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AGTT;AGTT) 0 common in clinvar
Chromosome3
Position3144644
GeneTRNT1
is asnp
is mentioned by
dbSNPrs1064796285
dbSNP (old)rs1064796285
ClinGenrs1064796285
ebirs1064796285
HLIrs1064796285
Exacrs1064796285
Gnomadrs1064796285
Varsomers1064796285
Maprs1064796285
PheGenIrs1064796285
Biobankrs1064796285
1000 genomesrs1064796285
hgdprs1064796285
ensemblrs1064796285
gopubmedrs1064796285
geneviewrs1064796285
scholarrs1064796285
googlers1064796285
pharmgkbrs1064796285
gwascentralrs1064796285
openSNPrs1064796285
23andMers1064796285
23andMe allrs1064796285
SNPshotrs1064796285
SNPdbers1064796285
MSV3drs1064796285
GWAS Ctlgrs1064796285
Max Magnitude0
ClinVar
Risk rs1064796285(-;-)
Alt rs1064796285(-;-)
Reference Rs1064796285(AGTT;AGTT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TRNT1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.3186328_3186331delTTAG
CLNSRC
CLNACC RCV000483978.1,