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rs771028677

From SNPedia

Orientationplus
Geno Mag Summary
(TTTG;TTTG) 0 common in clinvar
Make rs771028677(-;-)
Make rs771028677(-;TTTG)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61684053
GeneBRIP1
is asnp
is mentioned by
dbSNPrs771028677
ClinGenrs771028677
ebirs771028677
HLIrs771028677
Exacrs771028677
Varsomers771028677
Maprs771028677
PheGenIrs771028677
hapmaprs771028677
1000 genomesrs771028677
hgdprs771028677
ensemblrs771028677
gopubmedrs771028677
geneviewrs771028677
scholarrs771028677
googlers771028677
pharmgkbrs771028677
gwascentralrs771028677
openSNPrs771028677
23andMers771028677
23andMe allrs771028677
SNP Nexus

SNPshotrs771028677
SNPdbers771028677
MSV3drs771028677
GWAS Ctlgrs771028677
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs771028677(TTTG;TTTG)
Significance Pathogenic
Disease not provided Familial cancer of breast Fanconi anemia Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN not provided Familial cancer of breast Fanconi anemia, complementation group J Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.59761414_59761417delTTTG
CLNSRC Inc.
CLNACC RCV000214087.2, RCV000230820.1, RCV000234901.1,