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rs864622434

From SNPedia

Orientationplus
Make rs864622434(-;-)
Make rs864622434(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32319153
GeneBRCA2
is asnp
is mentioned by
dbSNPrs864622434
ebirs864622434
HLIrs864622434
Exacrs864622434
Varsomers864622434
Maprs864622434
PheGenIrs864622434
hapmaprs864622434
1000 genomesrs864622434
hgdprs864622434
ensemblrs864622434
gopubmedrs864622434
geneviewrs864622434
scholarrs864622434
googlers864622434
pharmgkbrs864622434
gwascentralrs864622434
openSNPrs864622434
23andMers864622434
23andMe allrs864622434
SNP Nexus

SNPshotrs864622434
SNPdbers864622434
MSV3drs864622434
GWAS Ctlgrs864622434
Max Magnitude
ClinVar
Risk rs864622434(;)
Alt rs864622434(;)
Reference rs864622434(A;A)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32893290delA
CLNSRC
CLNACC RCV000206144.2, RCV000214991.1,