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rs876659310

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGAATCCAGAAGGCCTTTC;AGAATCCAGAAGGCCTTTC) 0 common in clinvar
Make rs876659310(AGAATCCAGAAGGCCTTTC;TTT)
Make rs876659310(TTT;TTT)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43076554
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659310
dbSNP (old)rs876659310
ClinGenrs876659310
ebirs876659310
HLIrs876659310
Exacrs876659310
Gnomadrs876659310
Varsomers876659310
Maprs876659310
PheGenIrs876659310
Biobankrs876659310
1000 genomesrs876659310
hgdprs876659310
ensemblrs876659310
gopubmedrs876659310
geneviewrs876659310
scholarrs876659310
googlers876659310
pharmgkbrs876659310
gwascentralrs876659310
openSNPrs876659310
23andMers876659310
23andMe allrs876659310
SNP Nexus

SNPshotrs876659310
SNPdbers876659310
MSV3drs876659310
GWAS Ctlgrs876659310
Max Magnitude0
ClinVar
Risk rs876659310(TTT;TTT)
Alt rs876659310(TTT;TTT)
Reference Rs876659310(AGAATCCAGAAGGCCTTTC;AGAATCCAGAAGGCCTTTC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41228571_41228589del19insAAA
CLNSRC
CLNACC RCV000216050.1,