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rs864622536

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;A) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs864622536(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43093152
GeneBRCA1
is asnp
is mentioned by
dbSNPrs864622536
dbSNP (old)rs864622536
ClinGenrs864622536
ebirs864622536
HLIrs864622536
Exacrs864622536
Gnomadrs864622536
Varsomers864622536
Maprs864622536
PheGenIrs864622536
Biobankrs864622536
1000 genomesrs864622536
hgdprs864622536
ensemblrs864622536
gopubmedrs864622536
geneviewrs864622536
scholarrs864622536
googlers864622536
pharmgkbrs864622536
gwascentralrs864622536
openSNPrs864622536
23andMers864622536
23andMe allrs864622536
SNP Nexus

SNPshotrs864622536
SNPdbers864622536
MSV3drs864622536
GWAS Ctlgrs864622536
Max Magnitude6
ClinVar
Risk rs864622536(A;A)
Alt rs864622536(A;A)
Reference Rs864622536(-;-)
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.41245170dupT
CLNSRC
CLNACC RCV000204571.1, RCV000241437.1,