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rs864622302

From SNPedia

Merged intors80359264
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864622302(-;-)
Make rs864622302(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32332615
GeneBRCA2
is asnp
is mentioned by
dbSNPrs864622302
dbSNP (classic)rs864622302
ClinGenrs864622302
ebirs864622302
HLIrs864622302
Exacrs864622302
Gnomadrs864622302
Varsomers864622302
LitVarrs864622302
Maprs864622302
PheGenIrs864622302
Biobankrs864622302
1000 genomesrs864622302
hgdprs864622302
ensemblrs864622302
geneviewrs864622302
scholarrs864622302
googlers864622302
pharmgkbrs864622302
gwascentralrs864622302
openSNPrs864622302
23andMers864622302
SNPshotrs864622302
SNPdbers864622302
MSV3drs864622302
GWAS Ctlgrs864622302
StatusMerged into rs80359264
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs864622302(A;A)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32906753delA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000043744.4, RCV000077251.5, RCV000132193.2,