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rs397507964

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507964(-;-)
Make rs397507964(-;GTGG)
Make rs397507964(GTGG;GTGG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363377
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507964
ebirs397507964
HLIrs397507964
Exacrs397507964
Varsomers397507964
Maprs397507964
PheGenIrs397507964
hapmaprs397507964
1000 genomesrs397507964
hgdprs397507964
ensemblrs397507964
gopubmedrs397507964
geneviewrs397507964
scholarrs397507964
googlers397507964
pharmgkbrs397507964
gwascentralrs397507964
openSNPrs397507964
23andMers397507964
23andMe allrs397507964
SNP Nexus

SNPshotrs397507964
SNPdbers397507964
MSV3drs397507964
GWAS Ctlgrs397507964
Max Magnitude0
ClinVar
Risk rs397507964(TGGG;TGGG)
Alt rs397507964(TGGG;TGGG)
Reference rs397507964(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937511_32937514dupGTGG
CLNSRC ClinVar
CLNACC RCV000045440.2,