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rs773906955

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773906955(A;A)
Make rs773906955(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position35107026
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs773906955
ebirs773906955
HLIrs773906955
Exacrs773906955
Varsomers773906955
Maprs773906955
PheGenIrs773906955
hapmaprs773906955
1000 genomesrs773906955
hgdprs773906955
ensemblrs773906955
gopubmedrs773906955
geneviewrs773906955
scholarrs773906955
googlers773906955
pharmgkbrs773906955
gwascentralrs773906955
openSNPrs773906955
23andMers773906955
23andMe allrs773906955
SNP Nexus

SNPshotrs773906955
SNPdbers773906955
MSV3drs773906955
GWAS Ctlgrs773906955
Max Magnitude0
ClinVar
Risk rs773906955(A;A)
Alt rs773906955(A;A)
Reference rs773906955(G;G)
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 0
HGVS NC_000017.10:g.33434045G>A
CLNSRC
CLNACC RCV000215616.1,