Have questions? Visit https://www.reddit.com/r/SNPedia

rs397509190

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTAACCTT;CTAACCTT) 0 common in clinvar
Make rs397509190(-;-)
Make rs397509190(-;CTAACCTT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43099845
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509190
ebirs397509190
HLIrs397509190
Exacrs397509190
Varsomers397509190
Maprs397509190
PheGenIrs397509190
hapmaprs397509190
1000 genomesrs397509190
hgdprs397509190
ensemblrs397509190
gopubmedrs397509190
geneviewrs397509190
scholarrs397509190
googlers397509190
pharmgkbrs397509190
gwascentralrs397509190
openSNPrs397509190
23andMers397509190
23andMe allrs397509190
SNP Nexus

SNPshotrs397509190
SNPdbers397509190
MSV3drs397509190
GWAS Ctlgrs397509190
Max Magnitude0
ClinVar
Risk rs397509190(;)
Alt rs397509190(;)
Reference rs397509190(CTAACCTT;CTAACCTT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41251862_41251869delAAGGTTAG
CLNSRC ClinVar
CLNACC RCV000048638.2,