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rs397507984

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
(TA;TA) 0 common in clinvar
Make rs397507984(-;-)
Make rs397507984(-;AT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370485
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507984
ebirs397507984
HLIrs397507984
Exacrs397507984
Varsomers397507984
Maprs397507984
PheGenIrs397507984
hapmaprs397507984
1000 genomesrs397507984
hgdprs397507984
ensemblrs397507984
gopubmedrs397507984
geneviewrs397507984
scholarrs397507984
googlers397507984
pharmgkbrs397507984
gwascentralrs397507984
openSNPrs397507984
23andMers397507984
23andMe allrs397507984
SNP Nexus

SNPshotrs397507984
SNPdbers397507984
MSV3drs397507984
GWAS Ctlgrs397507984
Max Magnitude0
ClinVar
Risk rs397507984(;)
Alt rs397507984(;)
Reference rs397507984(TA;TA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32944622_32944623delAT
CLNSRC ClinVar
CLNACC RCV000045510.2,