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rs876660541

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;TTTT) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs876660541(TTTT;TTTT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32341057
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660541
dbSNP (classic)rs876660541
ClinGenrs876660541
ebirs876660541
HLIrs876660541
Exacrs876660541
Gnomadrs876660541
Varsomers876660541
LitVarrs876660541
Maprs876660541
PheGenIrs876660541
Biobankrs876660541
1000 genomesrs876660541
hgdprs876660541
ensemblrs876660541
geneviewrs876660541
scholarrs876660541
googlers876660541
pharmgkbrs876660541
gwascentralrs876660541
openSNPrs876660541
23andMers876660541
SNPshotrs876660541
SNPdbers876660541
MSV3drs876660541
GWAS Ctlgrs876660541
Max Magnitude6

aka c.6699_6702dupTTTT; however, rs876660541 has been merged into rs587781516

ClinVar
Risk rs876660541(TTTT;TTTT)
Alt rs876660541(TTTT;TTTT)
Reference Rs876660541(-;-)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32915191_32915194dupTTTT
CLNSRC
CLNACC RCV000215061.1,