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rs397507890

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTCGGT;TTCGGT) 0 common in clinvar
(TTTCGG;TTTCGG) 0 common in clinvar
Make rs397507890(-;-)
Make rs397507890(-;TTCGGT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32346893
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507890
ebirs397507890
HLIrs397507890
Exacrs397507890
Varsomers397507890
Maprs397507890
PheGenIrs397507890
hapmaprs397507890
1000 genomesrs397507890
hgdprs397507890
ensemblrs397507890
gopubmedrs397507890
geneviewrs397507890
scholarrs397507890
googlers397507890
pharmgkbrs397507890
gwascentralrs397507890
openSNPrs397507890
23andMers397507890
23andMe allrs397507890
SNP Nexus

SNPshotrs397507890
SNPdbers397507890
MSV3drs397507890
GWAS Ctlgrs397507890
Max Magnitude0
ClinVar
Risk rs397507890(;)
Alt rs397507890(;)
Reference rs397507890(TTTCGG;TTTCGG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32921030_32921035delTTCGGT
CLNSRC ClinVar
CLNACC RCV000045107.2,