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rs1064795352

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome17
Position61715995
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1064795352
dbSNP (old)rs1064795352
ClinGenrs1064795352
ebirs1064795352
HLIrs1064795352
Exacrs1064795352
Gnomadrs1064795352
Varsomers1064795352
Maprs1064795352
PheGenIrs1064795352
Biobankrs1064795352
1000 genomesrs1064795352
hgdprs1064795352
ensemblrs1064795352
gopubmedrs1064795352
geneviewrs1064795352
scholarrs1064795352
googlers1064795352
pharmgkbrs1064795352
gwascentralrs1064795352
openSNPrs1064795352
23andMers1064795352
23andMe allrs1064795352
SNPshotrs1064795352
SNPdbers1064795352
MSV3drs1064795352
GWAS Ctlgrs1064795352
Max Magnitude0
ClinVar
Risk rs1064795352(A;A)
Alt rs1064795352(A;A)
Reference Rs1064795352(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRIP1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.59793356C>T
CLNSRC
CLNACC RCV000485368.1,