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rs864622350

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;T) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs864622350(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43099790
GeneBRCA1
is asnp
is mentioned by
dbSNPrs864622350
ClinGenrs864622350
ebirs864622350
HLIrs864622350
Exacrs864622350
Varsomers864622350
Maprs864622350
PheGenIrs864622350
hapmaprs864622350
1000 genomesrs864622350
hgdprs864622350
ensemblrs864622350
gopubmedrs864622350
geneviewrs864622350
scholarrs864622350
googlers864622350
pharmgkbrs864622350
gwascentralrs864622350
openSNPrs864622350
23andMers864622350
23andMe allrs864622350
SNP Nexus

SNPshotrs864622350
SNPdbers864622350
MSV3drs864622350
GWAS Ctlgrs864622350
Max Magnitude6
ClinVar
Risk rs864622350(T;T)
Alt rs864622350(T;T)
Reference Rs864622350(-;-)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41251808dupA
CLNSRC
CLNACC RCV000203856.1, RCV000241120.1,