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rs730881935

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881935(-;-)
Make rs730881935(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position35107105
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs730881935
ClinGenrs730881935
ebirs730881935
HLIrs730881935
Exacrs730881935
Varsomers730881935
Maprs730881935
PheGenIrs730881935
hapmaprs730881935
1000 genomesrs730881935
hgdprs730881935
ensemblrs730881935
gopubmedrs730881935
geneviewrs730881935
scholarrs730881935
googlers730881935
pharmgkbrs730881935
gwascentralrs730881935
openSNPrs730881935
23andMers730881935
23andMe allrs730881935
SNP Nexus

SNPshotrs730881935
SNPdbers730881935
MSV3drs730881935
GWAS Ctlgrs730881935
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs730881935(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.33434124delT
CLNSRC
CLNACC RCV000160929.1,