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rs786202927

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202927(A;T)
Make rs786202927(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61683814
GeneBRIP1
is asnp
is mentioned by
dbSNPrs786202927
ebirs786202927
HLIrs786202927
Exacrs786202927
Varsomers786202927
Maprs786202927
PheGenIrs786202927
hapmaprs786202927
1000 genomesrs786202927
hgdprs786202927
ensemblrs786202927
gopubmedrs786202927
geneviewrs786202927
scholarrs786202927
googlers786202927
pharmgkbrs786202927
gwascentralrs786202927
openSNPrs786202927
23andMers786202927
23andMe allrs786202927
SNP Nexus

SNPshotrs786202927
SNPdbers786202927
MSV3drs786202927
GWAS Ctlgrs786202927
Max Magnitude0
ClinVar
Risk rs786202927(T;T)
Alt rs786202927(T;T)
Reference rs786202927(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59761175T>A
CLNSRC
CLNACC RCV000165998.1,