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rs1085307902

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position43104187
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1085307902
dbSNP (old)rs1085307902
ClinGenrs1085307902
ebirs1085307902
HLIrs1085307902
Exacrs1085307902
Gnomadrs1085307902
Varsomers1085307902
Maprs1085307902
PheGenIrs1085307902
Biobankrs1085307902
1000 genomesrs1085307902
hgdprs1085307902
ensemblrs1085307902
gopubmedrs1085307902
geneviewrs1085307902
scholarrs1085307902
googlers1085307902
pharmgkbrs1085307902
gwascentralrs1085307902
openSNPrs1085307902
23andMers1085307902
23andMe allrs1085307902
SNPshotrs1085307902
SNPdbers1085307902
MSV3drs1085307902
GWAS Ctlgrs1085307902
Max Magnitude0
ClinVar
Risk rs1085307902(T;T)
Alt rs1085307902(T;T)
Reference Rs1085307902(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.41256204G>A
CLNSRC
CLNACC RCV000489726.1,