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rs730881633

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881633(C;T)
Make rs730881633(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61801327
GeneBRIP1
is asnp
is mentioned by
dbSNPrs730881633
ebirs730881633
HLIrs730881633
Exacrs730881633
Varsomers730881633
Maprs730881633
PheGenIrs730881633
hapmaprs730881633
1000 genomesrs730881633
hgdprs730881633
ensemblrs730881633
gopubmedrs730881633
geneviewrs730881633
scholarrs730881633
googlers730881633
pharmgkbrs730881633
gwascentralrs730881633
openSNPrs730881633
23andMers730881633
23andMe allrs730881633
SNP Nexus

SNPshotrs730881633
SNPdbers730881633
MSV3drs730881633
GWAS Ctlgrs730881633
Max Magnitude0
ClinVar
Risk rs730881633(T;T)
Alt rs730881633(T;T)
Reference rs730881633(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000017.10:g.59878688G>A
CLNSRC
CLNACC RCV000160335.3, RCV000212307.1,