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rs1064793468

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome17
Position43092776
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1064793468
dbSNP (old)rs1064793468
ClinGenrs1064793468
ebirs1064793468
HLIrs1064793468
Exacrs1064793468
Gnomadrs1064793468
Varsomers1064793468
Maprs1064793468
PheGenIrs1064793468
Biobankrs1064793468
1000 genomesrs1064793468
hgdprs1064793468
ensemblrs1064793468
gopubmedrs1064793468
geneviewrs1064793468
scholarrs1064793468
googlers1064793468
pharmgkbrs1064793468
gwascentralrs1064793468
openSNPrs1064793468
23andMers1064793468
23andMe allrs1064793468
SNPshotrs1064793468
SNPdbers1064793468
MSV3drs1064793468
GWAS Ctlgrs1064793468
Max Magnitude0
ClinVar
Risk rs1064793468(GGGTG;GGGTG)
Alt rs1064793468(GGGTG;GGGTG)
Reference Rs1064793468(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.41244793_41244794insCACCC
CLNSRC
CLNACC RCV000482002.1,