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rs775171520

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs775171520(C;T)
Make rs775171520(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61793727
GeneBRIP1
is asnp
is mentioned by
dbSNPrs775171520
ebirs775171520
HLIrs775171520
Exacrs775171520
Varsomers775171520
Maprs775171520
PheGenIrs775171520
hapmaprs775171520
1000 genomesrs775171520
hgdprs775171520
ensemblrs775171520
gopubmedrs775171520
geneviewrs775171520
scholarrs775171520
googlers775171520
pharmgkbrs775171520
gwascentralrs775171520
openSNPrs775171520
23andMers775171520
23andMe allrs775171520
SNP Nexus

SNPshotrs775171520
SNPdbers775171520
MSV3drs775171520
GWAS Ctlgrs775171520
Max Magnitude0
ClinVar
Risk rs775171520(T;T)
Alt rs775171520(T;T)
Reference rs775171520(C;C)
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.59871088C>T
CLNSRC
CLNACC RCV000198848.3,