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rs397507577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAA;AAAA) 0 common in clinvar
Make rs397507577(-;-)
Make rs397507577(-;AAAA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332778
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507577
ebirs397507577
HLIrs397507577
Exacrs397507577
Varsomers397507577
Maprs397507577
PheGenIrs397507577
hapmaprs397507577
1000 genomesrs397507577
hgdprs397507577
ensemblrs397507577
gopubmedrs397507577
geneviewrs397507577
scholarrs397507577
googlers397507577
pharmgkbrs397507577
gwascentralrs397507577
openSNPrs397507577
23andMers397507577
23andMe allrs397507577
SNP Nexus

SNPshotrs397507577
SNPdbers397507577
MSV3drs397507577
GWAS Ctlgrs397507577
Max Magnitude0
ClinVar
Risk rs397507577(;)
Alt rs397507577(;)
Reference rs397507577(AAAA;AAAA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32906915_32906918delAAAA
CLNSRC ClinVar
CLNACC RCV000043776.2,