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rs1064794662

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position43049129
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1064794662
dbSNP (old)rs1064794662
ClinGenrs1064794662
ebirs1064794662
HLIrs1064794662
Exacrs1064794662
Gnomadrs1064794662
Varsomers1064794662
Maprs1064794662
PheGenIrs1064794662
Biobankrs1064794662
1000 genomesrs1064794662
hgdprs1064794662
ensemblrs1064794662
gopubmedrs1064794662
geneviewrs1064794662
scholarrs1064794662
googlers1064794662
pharmgkbrs1064794662
gwascentralrs1064794662
openSNPrs1064794662
23andMers1064794662
23andMe allrs1064794662
SNPshotrs1064794662
SNPdbers1064794662
MSV3drs1064794662
GWAS Ctlgrs1064794662
Max Magnitude0
ClinVar
Risk rs1064794662(-;-)
Alt rs1064794662(-;-)
Reference Rs1064794662(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.41201146delG
CLNSRC
CLNACC RCV000484335.1,