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rs781465150

From SNPedia

Merged intors80359775
Orientationplus
Stabilizedplus
Geno Mag Summary
(TGTA;TGTA) 0 common in clinvar
Make rs781465150(-;-)
Make rs781465150(-;TGTA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32398210
GeneBRCA2
is asnp
is mentioned by
dbSNPrs781465150
dbSNP (old)rs781465150
ClinGenrs781465150
ebirs781465150
HLIrs781465150
Exacrs781465150
Gnomadrs781465150
Varsomers781465150
Maprs781465150
PheGenIrs781465150
Biobankrs781465150
1000 genomesrs781465150
hgdprs781465150
ensemblrs781465150
gopubmedrs781465150
geneviewrs781465150
scholarrs781465150
googlers781465150
pharmgkbrs781465150
gwascentralrs781465150
openSNPrs781465150
23andMers781465150
23andMe allrs781465150
SNP Nexus

SNPshotrs781465150
SNPdbers781465150
MSV3drs781465150
GWAS Ctlgrs781465150
StatusMerged into rs80359775
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs781465150(TGTA;TGTA)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not specified
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not specified
Reversed 0
HGVS NC_000013.10:g.32972349_32972352delTATG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031843.9, RCV000131044.3, RCV000168365.3, RCV000200978.2,