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rs753023295

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs753023295(C;T)
Make rs753023295(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61780858
GeneBRIP1
is asnp
is mentioned by
dbSNPrs753023295
ebirs753023295
HLIrs753023295
Exacrs753023295
Varsomers753023295
Maprs753023295
PheGenIrs753023295
hapmaprs753023295
1000 genomesrs753023295
hgdprs753023295
ensemblrs753023295
gopubmedrs753023295
geneviewrs753023295
scholarrs753023295
googlers753023295
pharmgkbrs753023295
gwascentralrs753023295
openSNPrs753023295
23andMers753023295
23andMe allrs753023295
SNP Nexus

SNPshotrs753023295
SNPdbers753023295
MSV3drs753023295
GWAS Ctlgrs753023295
Max Magnitude0
ClinVar
Risk rs753023295(T;T)
Alt rs753023295(T;T)
Reference rs753023295(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRIP1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.59858219C>T
CLNSRC
CLNACC RCV000215063.1,