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rs1064793064

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTT;GTT) 0 common in clinvar
Chromosome13
Position32338000
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064793064
dbSNP (old)rs1064793064
ClinGenrs1064793064
ebirs1064793064
HLIrs1064793064
Exacrs1064793064
Gnomadrs1064793064
Varsomers1064793064
LitVarrs1064793064
Maprs1064793064
PheGenIrs1064793064
Biobankrs1064793064
1000 genomesrs1064793064
hgdprs1064793064
ensemblrs1064793064
gopubmedrs1064793064
geneviewrs1064793064
scholarrs1064793064
googlers1064793064
pharmgkbrs1064793064
gwascentralrs1064793064
openSNPrs1064793064
23andMers1064793064
23andMe allrs1064793064
SNPshotrs1064793064
SNPdbers1064793064
MSV3drs1064793064
GWAS Ctlgrs1064793064
Max Magnitude0
ClinVar
Risk rs1064793064(TA;TA)
Alt rs1064793064(TA;TA)
Reference Rs1064793064(GTT;GTT)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32912137_32912139delGTTinsTA
CLNSRC
CLNACC RCV000480422.1,