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rs137852985

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852985(A;A)
Make rs137852985(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position61808488
GeneBRIP1
is asnp
is mentioned by
dbSNPrs137852985
ebirs137852985
HLIrs137852985
Exacrs137852985
Varsomers137852985
Maprs137852985
PheGenIrs137852985
hapmaprs137852985
1000 genomesrs137852985
hgdprs137852985
ensemblrs137852985
gopubmedrs137852985
geneviewrs137852985
scholarrs137852985
googlers137852985
pharmgkbrs137852985
gwascentralrs137852985
openSNPrs137852985
23andMers137852985
23andMe allrs137852985
SNP Nexus

SNPshotrs137852985
SNPdbers137852985
MSV3drs137852985
GWAS Ctlgrs137852985
Max Magnitude0
OMIM605882
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852985(A;A)
Alt rs137852985(A;A)
Reference rs137852985(G;G)
Significance Pathogenic
Disease Breast cancer
Variation info
Gene BRIP1
CLNDBN Breast cancer, early-onset
Reversed 1
HGVS NC_000017.10:g.59885849C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005003.2,