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rs1064795955

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome1
Position100216024
GeneDBT
is asnp
is mentioned by
dbSNPrs1064795955
dbSNP (old)rs1064795955
ClinGenrs1064795955
ebirs1064795955
HLIrs1064795955
Exacrs1064795955
Gnomadrs1064795955
Varsomers1064795955
Maprs1064795955
PheGenIrs1064795955
Biobankrs1064795955
1000 genomesrs1064795955
hgdprs1064795955
ensemblrs1064795955
gopubmedrs1064795955
geneviewrs1064795955
scholarrs1064795955
googlers1064795955
pharmgkbrs1064795955
gwascentralrs1064795955
openSNPrs1064795955
23andMers1064795955
23andMe allrs1064795955
SNPshotrs1064795955
SNPdbers1064795955
MSV3drs1064795955
GWAS Ctlgrs1064795955
Max Magnitude0
ClinVar
Risk rs1064795955(-;-)
Alt rs1064795955(-;-)
Reference Rs1064795955(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DBT
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.100681580delG
CLNSRC
CLNACC RCV000480067.1,