Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064793572

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTTA;CTTA) 0 common in clinvar
Chromosome13
Position32332799
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064793572
dbSNP (old)rs1064793572
ClinGenrs1064793572
ebirs1064793572
HLIrs1064793572
Exacrs1064793572
Gnomadrs1064793572
Varsomers1064793572
LitVarrs1064793572
Maprs1064793572
PheGenIrs1064793572
Biobankrs1064793572
1000 genomesrs1064793572
hgdprs1064793572
ensemblrs1064793572
gopubmedrs1064793572
geneviewrs1064793572
scholarrs1064793572
googlers1064793572
pharmgkbrs1064793572
gwascentralrs1064793572
openSNPrs1064793572
23andMers1064793572
23andMe allrs1064793572
SNPshotrs1064793572
SNPdbers1064793572
MSV3drs1064793572
GWAS Ctlgrs1064793572
Max Magnitude0
ClinVar
Risk rs1064793572(-;-)
Alt rs1064793572(-;-)
Reference Rs1064793572(CTTA;CTTA)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32906936_32906939delACTT
CLNSRC
CLNACC RCV000484432.1,