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rs397508030

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508030(-;-)
Make rs397508030(-;TCTA)
Make rs397508030(TCTA;TCTA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379814
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508030
ebirs397508030
HLIrs397508030
Exacrs397508030
Varsomers397508030
Maprs397508030
PheGenIrs397508030
hapmaprs397508030
1000 genomesrs397508030
hgdprs397508030
ensemblrs397508030
gopubmedrs397508030
geneviewrs397508030
scholarrs397508030
googlers397508030
pharmgkbrs397508030
gwascentralrs397508030
openSNPrs397508030
23andMers397508030
23andMe allrs397508030
SNP Nexus

SNPshotrs397508030
SNPdbers397508030
MSV3drs397508030
GWAS Ctlgrs397508030
Max Magnitude0
ClinVar
Risk rs397508030(TCTA;TCTA)
Alt rs397508030(TCTA;TCTA)
Reference rs397508030(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32953951_32953952insTCTA
CLNSRC ClinVar
CLNACC RCV000045690.2,