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rs876658297

From SNPedia

Orientationminus
Geno Mag Summary
(TATG;TATG) 0 common in clinvar
Make rs876658297(-;-)
Make rs876658297(-;TATG)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position35107108
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs876658297
ebirs876658297
HLIrs876658297
Exacrs876658297
Varsomers876658297
Maprs876658297
PheGenIrs876658297
hapmaprs876658297
1000 genomesrs876658297
hgdprs876658297
ensemblrs876658297
gopubmedrs876658297
geneviewrs876658297
scholarrs876658297
googlers876658297
pharmgkbrs876658297
gwascentralrs876658297
openSNPrs876658297
23andMers876658297
23andMe allrs876658297
SNP Nexus

SNPshotrs876658297
SNPdbers876658297
MSV3drs876658297
GWAS Ctlgrs876658297
Max Magnitude0
ClinVar
Risk rs876658297(;)
Alt rs876658297(;)
Reference rs876658297(TATG;TATG)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.33434127_33434130delCATA
CLNSRC
CLNACC RCV000221453.1,