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rs770318608

From SNPedia

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


Make rs770318608(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32339929
GeneBRCA2
is asnp
is mentioned by
dbSNPrs770318608
ebirs770318608
HLIrs770318608
Exacrs770318608
Varsomers770318608
Maprs770318608
PheGenIrs770318608
hapmaprs770318608
1000 genomesrs770318608
hgdprs770318608
ensemblrs770318608
gopubmedrs770318608
geneviewrs770318608
scholarrs770318608
googlers770318608
pharmgkbrs770318608
gwascentralrs770318608
openSNPrs770318608
23andMers770318608
23andMe allrs770318608
SNP Nexus

SNPshotrs770318608
SNPdbers770318608
MSV3drs770318608
GWAS Ctlgrs770318608
Max Magnitude6
ClinVar
Risk rs770318608(;)
Alt rs770318608(;)
Reference rs770318608(AATT;AATT)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32914068_32914071delTTAA
CLNSRC Breast Cancer Information Core (BRCA2) Inc.
CLNACC RCV000031556.8, RCV000044684.5, RCV000131118.3, RCV000160296.2,