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rs398122670

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122670(-;-)
Make rs398122670(-;TC)
Make rs398122670(TC;TC)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092628
GeneBRCA1
is asnp
is mentioned by
dbSNPrs398122670
ebirs398122670
HLIrs398122670
Exacrs398122670
Varsomers398122670
Maprs398122670
PheGenIrs398122670
hapmaprs398122670
1000 genomesrs398122670
hgdprs398122670
ensemblrs398122670
gopubmedrs398122670
geneviewrs398122670
scholarrs398122670
googlers398122670
pharmgkbrs398122670
gwascentralrs398122670
openSNPrs398122670
23andMers398122670
23andMe allrs398122670
SNP Nexus

SNPshotrs398122670
SNPdbers398122670
MSV3drs398122670
GWAS Ctlgrs398122670
Max Magnitude0
ClinVar
Risk rs398122670(TC;TC)
Alt rs398122670(TC;TC)
Reference rs398122670(;)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Hereditary breast and ovarian cancer syndrome
Reversed 1
HGVS NC_000017.10:g.41244645_41244646insGA
CLNSRC ClinVar
CLNACC RCV000077119.2, RCV000204430.1,