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rs786202156

From SNPedia

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


Make rs786202156(AGG;AGG)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32326575
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202156
dbSNP (old)rs786202156
ClinGenrs786202156
ebirs786202156
HLIrs786202156
Exacrs786202156
Gnomadrs786202156
Varsomers786202156
Maprs786202156
PheGenIrs786202156
Biobankrs786202156
1000 genomesrs786202156
hgdprs786202156
ensemblrs786202156
gopubmedrs786202156
geneviewrs786202156
scholarrs786202156
googlers786202156
pharmgkbrs786202156
gwascentralrs786202156
openSNPrs786202156
23andMers786202156
23andMe allrs786202156
SNP Nexus

SNPshotrs786202156
SNPdbers786202156
MSV3drs786202156
GWAS Ctlgrs786202156
Max Magnitude6
ClinVar
Risk rs786202156(AGG;AGG)
Alt rs786202156(AGG;AGG)
Reference Rs786202156(TAGC;TAGC)
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.32900712_32900715delTAGCinsAGG
CLNSRC
CLNACC RCV000164830.1, RCV000241457.1,