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rs1064796683

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome5
Position177604396
GeneB4GALT7
is asnp
is mentioned by
dbSNPrs1064796683
dbSNP (old)rs1064796683
ClinGenrs1064796683
ebirs1064796683
HLIrs1064796683
Exacrs1064796683
Gnomadrs1064796683
Varsomers1064796683
Maprs1064796683
PheGenIrs1064796683
Biobankrs1064796683
1000 genomesrs1064796683
hgdprs1064796683
ensemblrs1064796683
gopubmedrs1064796683
geneviewrs1064796683
scholarrs1064796683
googlers1064796683
pharmgkbrs1064796683
gwascentralrs1064796683
openSNPrs1064796683
23andMers1064796683
23andMe allrs1064796683
SNPshotrs1064796683
SNPdbers1064796683
MSV3drs1064796683
GWAS Ctlgrs1064796683
Max Magnitude0
ClinVar
Risk rs1064796683(-;-)
Alt rs1064796683(-;-)
Reference Rs1064796683(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene B4GALT7
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.177031397delT
CLNSRC
CLNACC RCV000485451.1,