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rs1064793757

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome3
Position15635645
GeneBTD
is asnp
is mentioned by
dbSNPrs1064793757
dbSNP (old)rs1064793757
ClinGenrs1064793757
ebirs1064793757
HLIrs1064793757
Exacrs1064793757
Gnomadrs1064793757
Varsomers1064793757
Maprs1064793757
PheGenIrs1064793757
Biobankrs1064793757
1000 genomesrs1064793757
hgdprs1064793757
ensemblrs1064793757
gopubmedrs1064793757
geneviewrs1064793757
scholarrs1064793757
googlers1064793757
pharmgkbrs1064793757
gwascentralrs1064793757
openSNPrs1064793757
23andMers1064793757
23andMe allrs1064793757
SNPshotrs1064793757
SNPdbers1064793757
MSV3drs1064793757
GWAS Ctlgrs1064793757
Max Magnitude0
ClinVar
Risk rs1064793757(-;-)
Alt rs1064793757(-;-)
Reference Rs1064793757(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene BTD
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.15677152delA
CLNSRC
CLNACC RCV000482443.1,