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rs786204752

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;ACTTG) 6 BRCA2 variant considered pathogenic for breast cancer
(ACTTG;ACTTG) 0 common/normal
(GACTT;GACTT) 0 common in clinvar


Make rs786204752(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32337098
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786204752
dbSNP (old)rs786204752
ClinGenrs786204752
ebirs786204752
HLIrs786204752
Exacrs786204752
Gnomadrs786204752
Varsomers786204752
Maprs786204752
PheGenIrs786204752
Biobankrs786204752
1000 genomesrs786204752
hgdprs786204752
ensemblrs786204752
gopubmedrs786204752
geneviewrs786204752
scholarrs786204752
googlers786204752
pharmgkbrs786204752
gwascentralrs786204752
openSNPrs786204752
23andMers786204752
23andMe allrs786204752
SNP Nexus

SNPshotrs786204752
SNPdbers786204752
MSV3drs786204752
GWAS Ctlgrs786204752
Max Magnitude6
ClinVar
Risk rs786204752(-;-) Rs786204752(GACTT;GACTT)
Alt rs786204752(-;-) Rs786204752(GACTT;GACTT)
Reference Rs786204752(ACTTG;ACTTG)
Significance Other
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911235_32911239delACTTG
CLNSRC Counsyl
CLNACC RCV000169607.3, RCV000239268.1,