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rs1085307915

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome11
Position66698784
GeneSPTBN2
is asnp
is mentioned by
dbSNPrs1085307915
dbSNP (old)rs1085307915
ClinGenrs1085307915
ebirs1085307915
HLIrs1085307915
Exacrs1085307915
Gnomadrs1085307915
Varsomers1085307915
Maprs1085307915
PheGenIrs1085307915
Biobankrs1085307915
1000 genomesrs1085307915
hgdprs1085307915
ensemblrs1085307915
gopubmedrs1085307915
geneviewrs1085307915
scholarrs1085307915
googlers1085307915
pharmgkbrs1085307915
gwascentralrs1085307915
openSNPrs1085307915
23andMers1085307915
23andMe allrs1085307915
SNPshotrs1085307915
SNPdbers1085307915
MSV3drs1085307915
GWAS Ctlgrs1085307915
Max Magnitude0
ClinVar
Risk rs1085307915(G;G)
Alt rs1085307915(G;G)
Reference Rs1085307915(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPTBN2
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.66466255A>C
CLNSRC
CLNACC RCV000489542.1,