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rs786203318

From SNPedia

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


Make rs786203318(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32394784
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786203318
dbSNP (old)rs786203318
ClinGenrs786203318
ebirs786203318
HLIrs786203318
Exacrs786203318
Gnomadrs786203318
Varsomers786203318
Maprs786203318
PheGenIrs786203318
Biobankrs786203318
1000 genomesrs786203318
hgdprs786203318
ensemblrs786203318
gopubmedrs786203318
geneviewrs786203318
scholarrs786203318
googlers786203318
pharmgkbrs786203318
gwascentralrs786203318
openSNPrs786203318
23andMers786203318
23andMe allrs786203318
SNP Nexus

SNPshotrs786203318
SNPdbers786203318
MSV3drs786203318
GWAS Ctlgrs786203318
Max Magnitude6
ClinVar
Risk rs786203318(-;-)
Alt rs786203318(-;-)
Reference Rs786203318(AT;AT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32968921_32968922delAT
CLNSRC
CLNACC RCV000166577.1, RCV000241390.2, RCV000464242.1,