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rs397507747

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs397507747(-;-)
Make rs397507747(-;GT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326254
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507747
ebirs397507747
HLIrs397507747
Exacrs397507747
Varsomers397507747
Maprs397507747
PheGenIrs397507747
hapmaprs397507747
1000 genomesrs397507747
hgdprs397507747
ensemblrs397507747
gopubmedrs397507747
geneviewrs397507747
scholarrs397507747
googlers397507747
pharmgkbrs397507747
gwascentralrs397507747
openSNPrs397507747
23andMers397507747
23andMe allrs397507747
SNP Nexus

SNPshotrs397507747
SNPdbers397507747
MSV3drs397507747
GWAS Ctlgrs397507747
Max Magnitude0
ClinVar
Risk rs397507747(;)
Alt rs397507747(;)
Reference rs397507747(GT;GT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32900391_32900392delGT
CLNSRC ClinVar
CLNACC RCV000044513.2,