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rs797044987

From SNPedia

Orientationplus
Make rs797044987(AT;C)
Make rs797044987(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32339950
GeneBRCA2
is asnp
is mentioned by
dbSNPrs797044987
ebirs797044987
HLIrs797044987
Exacrs797044987
Varsomers797044987
Maprs797044987
PheGenIrs797044987
hapmaprs797044987
1000 genomesrs797044987
hgdprs797044987
ensemblrs797044987
gopubmedrs797044987
geneviewrs797044987
scholarrs797044987
googlers797044987
pharmgkbrs797044987
gwascentralrs797044987
openSNPrs797044987
23andMers797044987
23andMe allrs797044987
SNP Nexus

SNPshotrs797044987
SNPdbers797044987
MSV3drs797044987
GWAS Ctlgrs797044987
Max Magnitude
ClinVar
Risk rs797044987(C;C)
Alt rs797044987(C;C)
Reference rs797044987(AT;AT)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32914087_32914088delATinsC
CLNSRC
CLNACC RCV000190457.1,