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rs799908

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs799908(A;G)
Make rs799908(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43126899
GeneBRCA1
is asnp
is mentioned by
dbSNPrs799908
ebirs799908
HLIrs799908
Exacrs799908
Varsomers799908
Maprs799908
PheGenIrs799908
hapmaprs799908
1000 genomesrs799908
hgdprs799908
ensemblrs799908
gopubmedrs799908
geneviewrs799908
scholarrs799908
googlers799908
pharmgkbrs799908
gwascentralrs799908
openSNPrs799908
23andMers799908
23andMe allrs799908
SNP Nexus

SNPshotrs799908
SNPdbers799908
MSV3drs799908
GWAS Ctlgrs799908
GMAF0.444
Max Magnitude0


GET Evidence
rs799908
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.444444
summary



ClinVar
Risk rs799908(G;G)
Alt rs799908(G;G)
Reference rs799908(A;A)
Significance Non-pathogenic
Disease Breast-ovarian cancer
Variation info
Gene NBR2 BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 0
HGVS NC_000017.10:g.41278916A>G
CLNSRC
CLNACC RCV000191533.1,