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rs75096777

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(AA;AA) 0 common in clinvar
Make rs75096777(-;-)
Make rs75096777(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32331012
GeneBRCA2
is asnp
is mentioned by
dbSNPrs75096777
ebirs75096777
HLIrs75096777
Exacrs75096777
Varsomers75096777
Maprs75096777
PheGenIrs75096777
hapmaprs75096777
1000 genomesrs75096777
hgdprs75096777
ensemblrs75096777
gopubmedrs75096777
geneviewrs75096777
scholarrs75096777
googlers75096777
pharmgkbrs75096777
gwascentralrs75096777
openSNPrs75096777
23andMers75096777
23andMe allrs75096777
SNP Nexus

SNPshotrs75096777
SNPdbers75096777
MSV3drs75096777
GWAS Ctlgrs75096777
Max Magnitude0
ClinVar
Risk rs75096777(A,ATCAAA;A,ATCAAA)
Alt rs75096777(A,ATCAAA;A,ATCAAA)
Reference rs75096777(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32905149delA
CLNSRC ClinVar
CLNACC RCV000045305.2,