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rs1085307958

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome7
Position2544920
GeneBRAT1
is asnp
is mentioned by
dbSNPrs1085307958
dbSNP (old)rs1085307958
ClinGenrs1085307958
ebirs1085307958
HLIrs1085307958
Exacrs1085307958
Gnomadrs1085307958
Varsomers1085307958
Maprs1085307958
PheGenIrs1085307958
Biobankrs1085307958
1000 genomesrs1085307958
hgdprs1085307958
ensemblrs1085307958
gopubmedrs1085307958
geneviewrs1085307958
scholarrs1085307958
googlers1085307958
pharmgkbrs1085307958
gwascentralrs1085307958
openSNPrs1085307958
23andMers1085307958
23andMe allrs1085307958
SNPshotrs1085307958
SNPdbers1085307958
MSV3drs1085307958
GWAS Ctlgrs1085307958
Max Magnitude0
ClinVar
Risk rs1085307958(C;C)
Alt rs1085307958(C;C)
Reference Rs1085307958(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRAT1
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.2584554A>G
CLNSRC
CLNACC RCV000489648.1,