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rs397509207

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs397509207(AGA;TTTT)
Make rs397509207(TTTT;TTTT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43070967
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509207
ebirs397509207
HLIrs397509207
Exacrs397509207
Varsomers397509207
Maprs397509207
PheGenIrs397509207
hapmaprs397509207
1000 genomesrs397509207
hgdprs397509207
ensemblrs397509207
gopubmedrs397509207
geneviewrs397509207
scholarrs397509207
googlers397509207
pharmgkbrs397509207
gwascentralrs397509207
openSNPrs397509207
23andMers397509207
23andMe allrs397509207
SNP Nexus

SNPshotrs397509207
SNPdbers397509207
MSV3drs397509207
GWAS Ctlgrs397509207
Max Magnitude0
ClinVar
Risk rs397509207(TTTT;TTTT)
Alt rs397509207(TTTT;TTTT)
Reference rs397509207(AGA;AGA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41222984_41222986delTCTinsAAAA
CLNSRC ClinVar
CLNACC RCV000048704.2,