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rs574552037

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs574552037(A;A)
Make rs574552037(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position61716043
GeneBRIP1
is asnp
is mentioned by
dbSNPrs574552037
ebirs574552037
HLIrs574552037
Exacrs574552037
Varsomers574552037
Maprs574552037
PheGenIrs574552037
hapmaprs574552037
1000 genomesrs574552037
hgdprs574552037
ensemblrs574552037
gopubmedrs574552037
geneviewrs574552037
scholarrs574552037
googlers574552037
pharmgkbrs574552037
gwascentralrs574552037
openSNPrs574552037
23andMers574552037
23andMe allrs574552037
SNP Nexus

SNPshotrs574552037
SNPdbers574552037
MSV3drs574552037
GWAS Ctlgrs574552037
Max Magnitude0
ClinVar
Risk rs574552037(A,C;A,C)
Alt rs574552037(A,C;A,C)
Reference rs574552037(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia, complementation group J
Reversed 0
HGVS NC_000017.10:g.59793404G>A; NC_000017.10:g.59793404G>C
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000164130.1, RCV000228308.1, RCV000131417.3, RCV000205848.1,