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

rs786202700

From SNPedia

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


Make rs786202700(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32340217
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202700
dbSNP (old)rs786202700
ClinGenrs786202700
ebirs786202700
HLIrs786202700
Exacrs786202700
Gnomadrs786202700
Varsomers786202700
Maprs786202700
PheGenIrs786202700
Biobankrs786202700
1000 genomesrs786202700
hgdprs786202700
ensemblrs786202700
gopubmedrs786202700
geneviewrs786202700
scholarrs786202700
googlers786202700
pharmgkbrs786202700
gwascentralrs786202700
openSNPrs786202700
23andMers786202700
23andMe allrs786202700
SNP Nexus

SNPshotrs786202700
SNPdbers786202700
MSV3drs786202700
GWAS Ctlgrs786202700
Max Magnitude6
ClinVar
Risk rs786202700(-;-)
Alt rs786202700(-;-)
Reference Rs786202700(TT;TT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914354_32914355delTT
CLNSRC
CLNACC RCV000165639.1, RCV000241377.2,