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rs397507685

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
(TA;TA) 0 common in clinvar
Make rs397507685(-;-)
Make rs397507685(-;TA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338128
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507685
ebirs397507685
HLIrs397507685
Exacrs397507685
Varsomers397507685
Maprs397507685
PheGenIrs397507685
hapmaprs397507685
1000 genomesrs397507685
hgdprs397507685
ensemblrs397507685
gopubmedrs397507685
geneviewrs397507685
scholarrs397507685
googlers397507685
pharmgkbrs397507685
gwascentralrs397507685
openSNPrs397507685
23andMers397507685
23andMe allrs397507685
SNP Nexus

SNPshotrs397507685
SNPdbers397507685
MSV3drs397507685
GWAS Ctlgrs397507685
Max Magnitude0
ClinVar
Risk rs397507685(;)
Alt rs397507685(;)
Reference rs397507685(AT;AT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912265_32912266delTA
CLNSRC ClinVar
CLNACC RCV000044263.2,