Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064794202

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(TGTT;TGTT) 0 common in clinvar
Chromosome17
Position61859870
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1064794202
dbSNP (old)rs1064794202
ClinGenrs1064794202
ebirs1064794202
HLIrs1064794202
Exacrs1064794202
Gnomadrs1064794202
Varsomers1064794202
Maprs1064794202
PheGenIrs1064794202
Biobankrs1064794202
1000 genomesrs1064794202
hgdprs1064794202
ensemblrs1064794202
gopubmedrs1064794202
geneviewrs1064794202
scholarrs1064794202
googlers1064794202
pharmgkbrs1064794202
gwascentralrs1064794202
openSNPrs1064794202
23andMers1064794202
23andMe allrs1064794202
SNPshotrs1064794202
SNPdbers1064794202
MSV3drs1064794202
GWAS Ctlgrs1064794202
Max Magnitude0
ClinVar
Risk rs1064794202(-;-)
Alt rs1064794202(-;-)
Reference Rs1064794202(TGTT;TGTT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRIP1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.59937231_59937234delAACA
CLNSRC
CLNACC RCV000486415.1,