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rs730881943

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881943(-;-)
Make rs730881943(-;TA)
Make rs730881943(TA;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position35107440
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs730881943
ebirs730881943
HLIrs730881943
Exacrs730881943
Varsomers730881943
Maprs730881943
PheGenIrs730881943
hapmaprs730881943
1000 genomesrs730881943
hgdprs730881943
ensemblrs730881943
gopubmedrs730881943
geneviewrs730881943
scholarrs730881943
googlers730881943
pharmgkbrs730881943
gwascentralrs730881943
openSNPrs730881943
23andMers730881943
23andMe allrs730881943
SNP Nexus

SNPshotrs730881943
SNPdbers730881943
MSV3drs730881943
GWAS Ctlgrs730881943
Max Magnitude0
ClinVar
Risk rs730881943(TA;TA)
Alt rs730881943(TA;TA)
Reference rs730881943(;)
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.33434459_33434460insTA
CLNSRC
CLNACC RCV000160937.1,