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rs1064795577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome13
Position32337627
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064795577
dbSNP (classic)rs1064795577
ClinGenrs1064795577
ebirs1064795577
HLIrs1064795577
Exacrs1064795577
Gnomadrs1064795577
Varsomers1064795577
LitVarrs1064795577
Maprs1064795577
PheGenIrs1064795577
Biobankrs1064795577
1000 genomesrs1064795577
hgdprs1064795577
ensemblrs1064795577
geneviewrs1064795577
scholarrs1064795577
googlers1064795577
pharmgkbrs1064795577
gwascentralrs1064795577
openSNPrs1064795577
23andMers1064795577
23andMe allrs1064795577
SNPshotrs1064795577
SNPdbers1064795577
MSV3drs1064795577
GWAS Ctlgrs1064795577
Max Magnitude0
ClinVar
Risk rs1064795577(A;A)
Alt rs1064795577(A;A)
Reference Rs1064795577(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32911764T>A
CLNSRC
CLNACC RCV000479923.1,