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rs397508850

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508850(-;-)
Make rs397508850(-;AT)
Make rs397508850(AT;AT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094264
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508850
ebirs397508850
HLIrs397508850
Exacrs397508850
Varsomers397508850
Maprs397508850
PheGenIrs397508850
hapmaprs397508850
1000 genomesrs397508850
hgdprs397508850
ensemblrs397508850
gopubmedrs397508850
geneviewrs397508850
scholarrs397508850
googlers397508850
pharmgkbrs397508850
gwascentralrs397508850
openSNPrs397508850
23andMers397508850
23andMe allrs397508850
SNP Nexus

SNPshotrs397508850
SNPdbers397508850
MSV3drs397508850
GWAS Ctlgrs397508850
Max Magnitude0
ClinVar
Risk rs397508850(AT;AT)
Alt rs397508850(AT;AT)
Reference rs397508850(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246282_41246283dupAT
CLNSRC ClinVar
CLNACC RCV000047399.2,