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rs1064795172

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CGATT;CGATT) 0 common in clinvar
Chromosome13
Position32346875
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064795172
dbSNP (old)rs1064795172
ClinGenrs1064795172
ebirs1064795172
HLIrs1064795172
Exacrs1064795172
Gnomadrs1064795172
Varsomers1064795172
Maprs1064795172
PheGenIrs1064795172
Biobankrs1064795172
1000 genomesrs1064795172
hgdprs1064795172
ensemblrs1064795172
gopubmedrs1064795172
geneviewrs1064795172
scholarrs1064795172
googlers1064795172
pharmgkbrs1064795172
gwascentralrs1064795172
openSNPrs1064795172
23andMers1064795172
23andMe allrs1064795172
SNPshotrs1064795172
SNPdbers1064795172
MSV3drs1064795172
GWAS Ctlgrs1064795172
Max Magnitude0
ClinVar
Risk rs1064795172(-;-)
Alt rs1064795172(-;-)
Reference Rs1064795172(CGATT;CGATT)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32921012_32921016delCGATT
CLNSRC
CLNACC RCV000484185.1,