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rs760551339

From SNPedia

Orientationplus
Geno Mag Summary
(ATGG;ATGG) 0 common in clinvar
Make rs760551339(-;-)
Make rs760551339(-;ATGG)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61686054
GeneBRIP1
is asnp
is mentioned by
dbSNPrs760551339
ebirs760551339
HLIrs760551339
Exacrs760551339
Varsomers760551339
Maprs760551339
PheGenIrs760551339
hapmaprs760551339
1000 genomesrs760551339
hgdprs760551339
ensemblrs760551339
gopubmedrs760551339
geneviewrs760551339
scholarrs760551339
googlers760551339
pharmgkbrs760551339
gwascentralrs760551339
openSNPrs760551339
23andMers760551339
23andMe allrs760551339
SNP Nexus

SNPshotrs760551339
SNPdbers760551339
MSV3drs760551339
GWAS Ctlgrs760551339
Max Magnitude0
ClinVar
Risk rs760551339(;)
Alt rs760551339(;)
Reference rs760551339(ATGG;ATGG)
Significance Pathogenic
Disease Familial cancer of breast Fanconi anemia
Variation info
Gene BRIP1
CLNDBN Familial cancer of breast Fanconi anemia, complementation group J
Reversed 0
HGVS NC_000017.10:g.59763415_59763418delATGG
CLNSRC
CLNACC RCV000232131.1,